Endangered and Threatened Wildlife and Plants; Listing the Flying Earwig Hawaiian Damselfly and Pacific Hawaiian Damselfly As Endangered Throughout Their Ranges, 35990-36012 [2010-15237]
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SUMMARY: The FCC published a
document in the Federal Register of
June 15, 2010, (75 FR 33729), clarifying
the requirements necessary for
Broadband Radio Service (BRS) and
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licensees to demonstrate substantial
service and ensure that BRS licensees of
new initial licenses are given a
reasonable period of time to deploy
service, while ensuring that spectrum is
rapidly placed in use. The document
contained an incorrect page number in
reference to the BRS/EBS Third Further
Notice of Proposed Rulemaking citation.
DATES: Effective July 15, 2010.
FOR FURTHER INFORMATION CONTACT:
Nancy M. Zaczek, Wireless
Telecommunications Bureau,
Broadband Division, Federal
Communications Commission, 445 12th
Street, SW., Washington, DC 20554, at
(202) 418–0274 or via the Internet to
Nancy.Zaczek@fcc.gov.
Correction
In the Federal Register 75 FR 33729
published on Tuesday, June 15, 2010,
the following correction is made: On
page 33730, second column, paragraph
3, first sentence, remove the phrase ‘‘74
FR 49335’’ and insert ‘‘74 FR 49356.’’
Marlene H. Dortch,
Secretary, Federal Communications
Commission.
[FR Doc. 2010–15348 Filed 6–23–10; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R1-ES-2009-0036]
[MO 92210-0-0008]
RIN 1018-AV47
Endangered and Threatened Wildlife
and Plants; Listing the Flying Earwig
Hawaiian Damselfly and Pacific
Hawaiian Damselfly As Endangered
Throughout Their Ranges
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AGENCY: Fish and Wildlife Service,
Interior.
ACTION: Final rule.
SUMMARY: We, the U.S. Fish and
Wildlife Service (Service), determine
endangered status under the
Endangered Species Act of 1973, as
amended (Act), for two species of
Hawaiian damselflies, the flying earwig
Hawaiian damselfly (Megalagrion
nesiotes) on the island of Maui and the
Pacific Hawaiian damselfly (M.
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pacificum) on the islands of Hawaii,
Maui, and Molokai. This final rule
implements the Federal protections
provided by the Act for these species.
We also determine that critical habitat
for these two Hawaiian damselflies is
prudent, but not determinable at this
time.
DATES: This rule becomes effective July
26, 2010.
ADDRESSES: This final rule is available
on the Internet at https://
www.regulations.gov and https://
www.fws.gov/pacificislands. Comments
and materials received, as well as
supporting documentation used in the
preparation of this rule, will be
available for public inspection, by
appointment, during normal business
hours at: U.S. Fish and Wildlife Service,
Pacific Islands Fish and Wildlife Office,
300 Ala Moana Boulevard, Room 3-122,
Box 50088, Honolulu, HI 96850;
telephone, 808-792-9400; facsimile, 808792-9581.
FOR FURTHER INFORMATION CONTACT:
Loyal Mehrhoff, Field Supervisor,
Pacific Islands Fish and Wildlife Office
(see ADDRESSES). If you use a
telecommunications device for the deaf
(TDD), call the Federal Information
Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
Damselflies are insects in the order
Odonata, and are close relatives of
dragonflies, which they resemble in
appearance. Damselflies, however, are
slender-bodied and fold their wings
parallel to the body while at rest, which
readily distinguishes them from their
dragonfly relatives, which hold their
wings out perpendicular to the body
while not in flight.
The flying earwig Hawaiian damselfly
and the Pacific Hawaiian damselfly are
unique, endemic insects found only in
the Hawaiian Islands. Historically found
on the islands of Hawaii and Maui, the
flying earwig Hawaiian damselfly has
not been seen on the island of Hawaii
for over 80 years. Currently, the species
is known only from one location on
Maui. The Pacific Hawaiian damselfly
was historically found on all of the main
Hawaiian Islands except Kahoolawe and
Niihau. Currently, the Pacific Hawaiian
damselfly is known only from the
islands of Hawaii, Maui and Molokai.
The Hawaiian Islands are well known
for several spectacular evolutionary
radiations (the rapid evolution of new
species from a single ancestral type, as
a result of adaptation and divergence in
response to new ecological conditions)
resulting in unique insect fauna found
nowhere else in the world. One such
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group, which began its evolution
perhaps as long as 10 million years ago
(Jordan et al. 2003, p. 89), is the narrowwinged Hawaiian damselfly genus
Megalagrion. This genus appears to be
most closely related to species of
Pseudagrion elsewhere in the IndoPacific (Zimmerman 1948a, pp. 341,
345). The Megalagrion species of the
Hawaiian Islands have evolved to
occupy as many larval breeding niches
(different adaptations and ecological
conditions for breeding and
development of larvae, including
chemical, physical, spatial, and
temporal factors) as all the rest of the
world’s damselfly species combined,
and in terms of the number of insularendemic (native to only one island)
species, are exceeded only by the
radiation of damselfly species of Fiji in
the Pacific (Jordan et al. 2003, p. 91).
Native Hawaiians apparently did not
differentiate the various species, but
referred to the native damselflies (and
dragonflies) collectively as ‘‘pinao,’’ and
to the red-colored damselflies
specifically as ‘‘pinao ula.’’ There has
been no traditional European use of a
common name for species in the genus
Megalagrion. In his 1994 taxonomic
review of the candidate species of
insects of the Hawaiian Islands, Nishida
(1994, pp. 4-7) proposed the name
‘‘Hawaiian damselflies’’ as the common
name for species in the genus
Megalagrion. Because this name reflects
the restricted distribution of these
insects and is nontechnical, the
common name ‘‘Hawaiian damselflies’’
is adopted for general use here, and we
use the common names flying earwig
Hawaiian damselfly and Pacific
Hawaiian damselfly to identify the two
species addressed in this final rule.
The general biology of Hawaiian
damselflies is typical of other narrowwinged damselflies (Polhemus and
Asquith 1996, pp. 2-7). The males of
most species are territorial, guarding
areas of habitat where females lay eggs
(Moore 1983a, p. 89). During copulation,
and often while the female lays eggs, the
male grasps the female behind the head
with terminal abdominal appendages to
guard the female against rival males;
thus males and females are frequently
seen flying in tandem.
Female damselflies lay eggs in
submerged aquatic vegetation or in mats
of moss or algae on submerged rocks,
and hatching occurs in about 10 days
(Williams 1936, pp. 303, 306, 318;
Evenhuis et al. 1995, p. 18). In most
species of Hawaiian damselflies, the
immature larval stages (naiads) are
aquatic, breathing through three
flattened abdominal gills, and are
predaceous, feeding on small aquatic
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invertebrates or fish (Williams 1936, p.
303). Naiads may take up to 4 months
to mature (Williams 1936, p. 309), after
which they crawl out of the water onto
rocks or vegetation to molt into winged
adults, typically remaining close to the
aquatic habitat from which they
emerged. The Pacific Hawaiian
damselfly exhibits this typical aquatic
life history.
In contrast, the naiads of a few species
of Hawaiian damselflies are terrestrial or
semiterrestrial, living on wet rock faces
or in damp terrestrial conditions,
inhabiting wet leaf litter or moist leaf
axils (the angled juncture of the leaf and
stem) of native plants up to several feet
above ground (Zimmerman 1970, p. 33;
Simon et al. 1984, p. 13; Polhemus and
Asquith 1996, p. 17). The naiads of
these terrestrial and semiterrestrial
species have evolved short, thick, hairy
gills and in many species are unable to
swim (Polhemus and Asquith 1996, p.
75). The flying earwig Hawaiian
damselfly is believed to exhibit this
terrestrial or semiterrestrial naiad life
history.
The Hawaiian damselflies are
represented by 23 species and 5
subspecies, and are currently found on
6 of the Hawaiian Islands (Kauai, Oahu,
Molokai, Maui, Lanai, and Hawaii).
There are more species of Megalagrion
on the geologically older islands (12
species on Kauai) than on the
geologically youngest island (8 species
on Hawaii), and there are more singleisland endemic species on the older
islands (10 on Kauai) than on the
youngest island (none on Hawaii)
(Jordan et al. 2003, p. 91). Historically,
Megalagrion damselflies were among
the most common and conspicuous
native Hawaiian insects. Some species
commonly inhabited water gardens in
residential areas, artificial reservoirs,
and watercress farms, and were even
abundant in the city of Honolulu, as
noted by early collectors of this group
(Perkins 1899, p. 76; Perkins 1913, p.
clxxviii; Williams 1936, p. 304).
Beginning with the extensive stream
and wetland conversion, alteration, and
modification, and degradation of native
forests through the 20th century,
Hawaii’s native damselflies, including
the two species that are the subject of
this final listing action, experienced a
tremendous reduction in available
habitat. In addition, predation by a
number of nonnative species that have
been both intentionally and, in some
cases, inadvertently introduced into the
Hawaiian Islands is a significant and
ongoing threat to all native Hawaiian
damselflies.
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Previous Federal Actions
Both the flying earwig Hawaiian
damselfly and the Pacific Hawaiian
damselfly were first designated as
candidate species on May 22, 1984 (49
FR 21664). Candidate species are those
taxa for which the Service has sufficient
information on their biological status
and threats to propose them for listing
under the Act (16 U.S.C. 1531 et seq.),
but for which the development of a
listing regulation has been precluded by
other higher-priority listing activities.
The flying earwig Hawaiian damselfly
was removed from the candidate list on
November 21, 1991 (56 FR 58804),
whereas the Pacific Hawaiian damselfly
retained its status as a candidate
species. On November 15, 1994 (59 FR
58982), the flying earwig Hawaiian
damselfly was added back onto the
candidate list. In the Candidate Notice
of Review (CNOR) published on
February 28, 1996 (61 FR 7595), we
announced a revised list of plant and
animal taxa that we regarded as
candidates for possible addition to the
Lists of Threatened and Endangered
Wildlife and Plants. This revision also
included a new ranking system,
whereby each candidate species was
assigned a Listing Priority Number
(LPN) from 1 to 12. Both the flying
earwig Hawaiian damselfly and the
Pacific Hawaiian damselfly were
assigned an LPN of 2 on February 28,
1996 (61 FR 7595).
On May 4, 2004, the Center for
Biological Diversity petitioned the
Secretary of the Interior to list 225
species of plants and animals that were
already candidates, including these two
Hawaiian damselfly species, as
endangered or threatened under the
provisions of the Act. In our annual
CNOR, dated May 11, 2005 (70 FR
24870), we retained a listing priority
number of 2 for both of these species in
accordance with our listing priority
guidance published on September 21,
1983 (48 FR 43098). A listing priority
number of 2 reflects threats that are both
imminent and high in magnitude, as
well as the taxonomic classification of
each of these two Hawaiian damselflies
as distinct species. At the time, we
determined that publication of a
proposed rule to list these species was
precluded by our work on higher
priority listing actions. Since then, we
have published our annual findings on
the May 4, 2004, petition (including our
findings on these two candidate species)
in the CNORs dated September 12, 2006
(71 FR 53756), December 6, 2007 (72 FR
69034), and December 10, 2008 (73 FR
75176).
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35991
In fiscal year 2007, we determined
that funding was available to initiate
work on listing determinations for these
two species. On July 8, 2009, we
published a proposed rule to list the
flying earwig Hawaiian damselfly and
the Pacific Hawaiian damselfly as
endangered (74 FR 32490). We solicited
data and comments from the public on
the proposed rule for 60 days, ending
September 8, 2009. To allow the public
and interested parties additional time to
submit comments on the proposed rule,
we reopened the comment period on
November 19, 2009 (74 FR 59956), and
accepted comments until December 21,
2009.
Species Information
Flying Earwig Hawaiian Damselfly
The flying earwig Hawaiian damselfly
was first described from specimens
collected in the 1890s in Puna on
Hawaii Island by R.C.L. Perkins (1899,
p. 72). Kennedy (1934, pp. 343-345)
described what was believed at the time
to be a new species of damselfly based
on specimens from Maui; these were
later determined to be synonymous with
the specimens collected by Perkins. The
flying earwig Hawaiian damselfly is a
comparatively large and elongated
species. The males are blue and black in
color and exhibit distinctive, greatly
enlarged, pincer-like cerci (paired
appendages on the rearmost segment of
the abdomen used to clasp the female
during mating). It is for the males’
elongated abdominal appendages and
their resemblance to those found on
earwigs (order Dermaptera) that the
species is named. Females are
predominantly brownish in color. The
adults measure from 1.8 to 1.9 inches
(in) (46 to 50 millimeters (mm)) in
length and have a wingspan of 1.9 to 2.1
in (50 to 53 mm). The wings of both
sexes are clear except for the tips, which
are narrowly darkened along the front
margins. Naiads of this species have
never been collected or found
(Polhemus and Asquith 1996, p. 69), but
they are believed to be terrestrial or
semiterrestrial in habit (Kennedy 1934,
p. 345; Preston 2007a).
The biology of the flying earwig
Hawaiian damselfly is not well
understood, and it is unknown if this
species is more likely to be associated
with standing water or flowing water
(Kennedy 1934, p. 345; Polhemus 1994,
p. 40). The only confirmed population
found in the last 6 years occurs along a
single East Maui stream and the
adjacent steep, moist, riparian talus
slope (a slope formed by an
accumulation of rock debris), which is
densely covered with Dicranopteris
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linearis (uluhe), a native fern. Adults of
the flying earwig Hawaiian damselfly
have been observed to perch on
vegetation and boulders, and to fly
slowly for short distances above this
particular stream within the one known
remaining habitat site. When disturbed,
the adults fly downward within nearby
vegetation or between rocks, rather than
up and away as is usually observed with
aquatic Hawaiian damselfly species.
Although immature individuals have
not been located, based on the habitat
and the behavior of the adults, it is
believed that the naiads may be
terrestrial or semiterrestrial, occurring
among damp leaflitter (Kennedy 1934,
p. 345) or possibly within moist soil or
seeps between boulders in suitable
habitat (Preston 2007a). The highest
elevation at which this species has been
recorded is 3,000 feet (ft) (914 meters
(m)), but its close association with uluhe
habitat suggests that its range may
extend upward to close to 4,000 ft
(1,212 m) (Foote 2007).
Historically, the flying earwig
Hawaiian damselfly was known from
the islands of Hawaii and Maui. On
Hawaii, it was originally known from
seven or more general localities. The
species has not been seen on Hawaii for
over 80 years, although extensive
surveys within apparently suitable
habitat in the Kau and Olaa areas were
conducted from 1997 to 2008 (Polhemus
2008). On Maui, the flying earwig
damselfly was historically reported from
five general locations on the windward
side of the island (Kennedy 1934, p.
345). Since the 1930s, however, the
flying earwig Hawaiian damselfly has
only been observed in a single area
along a particular stream on the
windward side of east Maui, despite
surveys from 1993 through 2008 at
several of its historically occupied sites.
Although presumed extant, the last
observation of the species was in 2005
(Foote 2008); the species was not
observed during the last survey at this
location in 2008. No quantitative
estimate of the size of this remaining
population is available.
It is hypothesized that the flying
earwig Hawaiian damselfly may now be
restricted to what is perhaps suboptimal
habitat, where periodic absences of the
species due to drought may be expected
and might explain the lack of
observations of the species (Foote 2007).
Some researchers also believe that
overcollection of this species by
enthusiasts may have impacted some
populations in the past (Polhemus
2008). It is further possible that the
individuals observed in this area are
actually part of a larger population that
may be located in the extensive belt of
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uluhe habitat located upslope, where
the habitat is predominantly native
shrubs and matted fern understory
(Foote 2007; Hawaii Biodiversity and
Mapping Program (HBMP) 2006).
Unsurveyed areas containing potentially
suitable habitat for this species include
the Hana coast of east Maui, and the east
rift zone of Kilauea and the Kona area
on the island of Hawaii (Foote 2007).
Pacific Hawaiian Damselfly
The Pacific Hawaiian damselfly was
first described by McLachlan (1883, p.
234), based on specimens collected by
R.C.L. Perkins from streams on the
islands of Lanai and Maui. This
damselfly is a relatively small, darkcolored species, with adults measuring
1.3 to 1.4 in (34 to 37 mm) in length and
having a wingspan of 1.3 to 1.6 in (33
to 42 mm). Both adult males and
females are mostly black in color. Males
exhibit brick-red striping and patterns,
while females exhibit light-green
striping and patterns. The only
immature individuals of this species
that have been collected were earlyinstar (an intermoult stage of
development) individuals, and they
exhibit flattened, leaf-like gills
(Polhemus and Asquith 1996, p. 83).
This species is most easily
distinguished from other Hawaiian
damselflies by the extremely long lower
abdominal appendages of the male,
which greatly exceed the length of the
upper appendages.
Historically, the Pacific Hawaiian
damselfly was known from lower
elevations (below 2,000 ft (600 m)) on
all of the main Hawaiian Islands except
Kahoolawe and Niihau (Perkins 1899, p.
64). This species was known to breed
primarily in lentic (standing water)
systems such as marshes, seepage-fed
pools, large ponds at higher elevations,
and small, quiet pools in gulches that
have been cut off from the main stream
channel (Moore and Gagne 1982, p. 4;
Polhemus and Asquith 1996, p. 83). The
Pacific Hawaiian damselfly is no longer
found in most lentic habitats in Hawaii,
such as ponds and taro (Colocasia
esculenta) fields, due to predation by
nonnative fish that now occur in these
systems (Moore and Gagne 1982, p. 4;
Englund et al. 2007, p. 215).
Observations have confirmed that the
Pacific Hawaiian damselfly is now
restricted almost exclusively to seepagefed pools along overflow channels in the
terminal reaches of perennial streams,
usually in areas surrounded by thick
vegetation (Moore and Gagne 1982, pp.
3-4; Polhemus 1994, p. 54; Englund
1999, p. 236; Englund et al. 2007, p.
216; Polhemus 2007, p. 238). Adults
usually do not stray far from the vicinity
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of the breeding pools, perching on
bordering vegetation and flying only
short distances when disturbed
(Polhemus and Asquith 1996, p. 83).
This species is rarely seen along main
stream channels, and its ability to
disperse long distances over land or
water is suspected to be poor compared
to other Hawaiian damselflies (Jordan et
al. 2007, p. 254).
The Pacific Hawaiian damselfly is
now believed to be extirpated from the
islands of Oahu, Kauai, and Lanai
(Polhemus and Asquith 1996, p. 83). On
the island of Oahu, due to its
occupation of particularly vulnerable
habitat within sidepools of lowland
streams, the Pacific Hawaiian damselfly
was rare by the 1890s and appears to
have been extirpated from this island by
1910 (Liebherr and Polhemus 1997, p.
494). It is unknown when the Kauai and
Lanai populations of the Pacific
Hawaiian damselfly disappeared. Until
1998, it was believed that the species
was extirpated from the island of
Hawaii. That year, one population was
discovered within a small stream
located just above, but isolated from,
Maili Stream, which is known to be
occupied by nonnative fish (Englund
1998, pp. 15-16). On Maui and Molokai,
fewer than six populations of the Pacific
Hawaiian damselfly could be located by
the 1970s (Harwood 1976, pp. 251-253;
Gagne 1980, pp. 119, 125; Moore and
Gagne 1982, p. 1). The conservation of
this species was identified as a priority
by the International Union for the
Conservation of Nature and Natural
Resources (Moore 1982, p. 209).
The Pacific Hawaiian damselfly is
currently found in at least seven streams
on Molokai and may possibly be extant
in other unsurveyed streams on
Molokai’s northern coast that have not
been invaded by nonnative fish
(Englund 2008). On the island of Maui,
the species is currently known from 14
streams. The Pacific Hawaiian damselfly
is no longer found along the entire
reaches of these Maui streams, but only
in restricted areas along each stream
where steep terrain prevents access by
nonnative fish, which inhabit degraded,
lower stream reaches (Polhemus and
Asquith 1996, p. 13; Englund et al.
2007, p. 215). The species is known
from a single population on the island
of Hawaii, last observed in 1998.
No quantitative estimates of the size
of the extant populations are available.
Howarth (1991, p. 490) described the
Pacific Hawaiian damselfly as the most
common and most widespread of the
native damselfly species at the end of
the 19th century, and yet a decline in
this species was observed as early as
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1905 due to the effects of nonnative fish
introduced for control of mosquitoes.
Summary of Comments and
Recommendations
In our proposed rule published on
July 8, 2009 (74 FR 32490), we
requested that all interested parties
submit written comments on the
proposal by September 8, 2009. We also
contacted appropriate Federal and State
agencies, scientific experts and
organizations, and other interested
parties and invited them to comment on
the proposal. Newspaper notices
inviting general public comment were
published on the islands of Hawaii,
Maui, Molokai, and Oahu. On
November 19, 2009 (74 FR 59956), we
reopened the comment period for an
additional 30 days, ending December
21, 2009.
We received a total of five written
comments and no requests for public
hearings. Three comments were from
State of Hawaii agencies and two were
from the same nongovernmental
organization. We received three
comments supporting the listing of the
two Hawaiian damselflies. Two
comments neither supported nor
opposed the listings, and one of these
comments provided additional
information on the two damselflies. We
also requested peer review from
potential peer reviewers.
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Peer Review Comments
In accordance with our peer review
policy published on July 1, 1994 (59 FR
34270), we solicited expert opinion
from seven knowledgeable individuals
with scientific expertise that included
familiarity with the two Hawaiian
damselflies and their habitat, biological
needs, and threats. We received no
written comments from any of the seven
peer reviewers, although several offered
their opinion that the two Hawaiian
damselfly species meet the definition of
an endangered species (A. Asquith,
Hawaii Sea Grant, pers. comm. 2009; F.
Howarth, Bishop Museum, pers. comm.
2009; K. Magnacca, University of
Hawaii at Hilo, pers. comm. 2009; D.
Polhemus, State of Hawaii Division of
Aquatic Resources, pers. comm. 2009;
D. Preston, Bishop Museum, pers.
comm. 2009).
Comments from the State of Hawaii
The State of Hawaii’s State Historic
Preservation Division concurred that no
historic properties would be affected by
the listing of the two Hawaiian
damselflies (McMahon 2009, pers.
comm.). The State’s Division of Forestry
and Wildlife (DOFAW) and Office of
Hawaiian Affairs supported listing the
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two damselflies as endangered (Conry
2009, pers. comm.; Namu’o 2009, pers.
comm.).
Public Comments
(1) Comment: One commenter stated
that there appears to be little, if any,
empirical data indicating water
diversions have any potential impact on
the flying earwig Hawaiian damselfly.
Our response: While we acknowledge
that the larval stage of the flying earwig
Hawaiian damselfly has never been
observed within stream water, repeated
observations of the adults along the
stream adjacent to its only known
population site on east Maui indicate a
strong biological association of an
unknown nature with flowing stream
water. This association is likely related
to the species’ natural history and may
include the need for sufficient space or
a stream setting for mating adults and
territorial behavior of males.
Additionally, the species’ larval habitat
is undoubtedly dependent on localized
area hydrology. For example, should a
stream experience either reduced flow
or complete dewatering for an extended
period of time, it is expected that the
impact to surrounding soils and
associated vegetation, including the
uluhe ferns that are believed to be the
species’ likely larval-stage habitat, will
be soil desiccation and concomitant
prolonged vegetation dieback, resulting
in degraded habitat conditions for the
flying earwig Hawaiian damselfly.
(2) Comment: One commenter stated
the reduction or modification of water
flow in a stream should not be
identified as an activity that could
potentially result in violation of section
9 of the Act pertaining to the flying
earwig Hawaiian damselfly.
Our response: As discussed in the
previous response (see Comment 1), we
believe there is a strong association with
stream water flow and the species’ life
history requirements. Stream flow is
likely essential to the adult damselfly’s
breeding requirements and is also
essential to maintaining localized soil
hydrology necessary for persistence of
uluhe ferns, which are known foraging
and mating sites for the adults and may
provide habitat for the larval stage.
Therefore, any permanent or prolonged
reduction or modification of stream flow
in a stream utilized by this species may
result in a violation of section 9 of the
Act.
(3) Comment: One commenter stated
that distribution of both species is not
fully known and recommended that the
Service conduct additional surveys for
both species prior to proceeding with
listing.
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35993
Our response: In preparing both the
proposed and final rules for these
species, we reviewed the best scientific
and commercial data available,
including technical reports, published
journal articles, and numerous other
documents, including unpublished
reports and surveys. In addition, we
consulted with several species experts.
We based our listing determination for
the flying earwig Hawaiian damselfly
and the Pacific Hawaiian damselfly on
the best available information regarding
the species’ current known population
status, the known condition of their
habitat, and the current factors affecting
the species, along with ongoing
conservation efforts, as described in the
Summary of Factors Affecting the
Species (below) in this final rule. The
Act neither provides for, nor requires,
additional research effort prior to a
listing decision. We acknowledge that
uncertainties exist; however, under
section 4 of the Act, we must make a
listing determination based on the best
scientific and commercial available at
the time of our determination.
(4) Comment: One commenter
disagreed with our analysis that stream
diversions for agriculture have reduced
stream habitat available to the Pacific
Hawaiian damselfly, and currently pose
a threat to this species.
Our response: Historically, the
impacts of the plantation-era sugarcane
irrigation system reduced stream habitat
available to this species. The Pacific
Hawaiian damselfly was once among
the most commonly observed aquatic
insects in the islands (Zimmerman
1948, p. 377). Because this species
breeds in lentic habitats or stream
terminal reaches, which experienced
significant modification for agriculture
beginning as early as the 19th century,
the Pacific Hawaiian damselfly was
extirpated from many of its historical
habitat sites (Polhemus 2007, p. 236). By
the 1930s, water diversions had been
developed on all of the main Hawaiian
Islands, and by 1978, the stream flow in
over one-half of all of the 366 perennial
streams in Hawaii had been altered in
some manner (Brasher 2003, p. 1055).
All or most of the low or average flow
of the stream was, and often still is,
diverted into fields or reservoirs, leaving
many stream channels completely dry
(Takasaki et al. 1969, pp. 27-28; Harris
et al. 1993, p. 12; Wilcox 1996, p. 56).
With the nearly complete cessation of
this industry in the Hawaiian Islands, it
is unlikely that new irrigation-related
water diversion activities will be
initiated in the remaining streams that
currently provide habitat for the Pacific
Hawaiian damselfly. However, most of
the historical water diversions remain in
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place. The historical loss of stream
habitat, resulting in the present
curtailment of habitat available to the
Pacific Hawaiian damselfly, combined
with the threat of predation by
nonnative fish in the remaining stream
habitat, continues to restrict and reduce
the amount of habitat potentially
available to this species. Should some of
this water be returned to stream
systems, the amount of habitat available
to this species may increase if the water
return were to be implemented carefully
to prevent the spread of nonnative fish
species upstream.
(5) Comment: One commenter noted
the Pacific Hawaiian damselfly,
although historically known from lower
elevations, is now known to have
established successfully breeding
populations at higher elevations above
existing stream diversions.
Our response: Prior to the
establishment of widespread stream
diversions, the Pacific Hawaiian
damselfly was considered one of the
most abundant and frequently observed
insects in Hawaii and was known from
all of the main Hawaiian Islands, except
Kahoolawe and Niihau. Previously
known from suitable portions of many
streams and water bodies from sea level
to some higher elevation sites
(Zimmerman 1948, p. 377), the Pacific
Hawaiian damselfly is now extirpated
from at least 18 known population sites
on the islands of Hawaii, Kauai, Lanai,
Oahu, Maui, and Molokai. Diversions
changed the amount and flow rate of
water within many lower stream
sections, because the diversions either
reduced the amount of water flow at the
point of diversion, or captured all
stream water (as they were designed to
do) during times of drier weather or
drought. The Pacific Hawaiian
damselfly is currently found in
approximately 22 streams on the islands
of Hawaii, Maui, and Molokai, across a
variety of elevations. All known
populations are located within streams
or bodies of water free of nonnative,
predatory fish. We lack sufficient
information to determine whether all
stream reaches occupied by this
damselfly species are now above
manmade diversions, but we know the
species is largely absent from areas
below manmade diversions.
(6) Comment: One commenter stated
that the current known range of the
Pacific Hawaiian damselfly appears to
be broader than the species’ known
range at the time it became a candidate
for listing.
Our response: We acknowledged in
our proposed rule that at the time we
determined we had sufficient
information on file to support a
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proposal to list the Pacific Hawaiian
damselfly (1984), and elevated it to
candidate status, it had been extirpated
from Kauai, Oahu, and Lanai, and was
also considered extirpated from the
island of Hawaii. Subsequently in 1998,
a single population was discovered on
an isolated portion of a Hilo stream on
the island of Hawaii. However, since
then, the Pacific Hawaiian damselfly
has not been reobserved on Kauai,
Lanai, or Oahu, and remains only on
Molokai and Maui, and one location on
Hawaii Island. We do not consider the
discovery of a single population on the
island of Hawaii to represent a
significant broadening of the range of
the species.
(7) Comment: One commenter
observed that water diversions may
enhance the damselflies’ chances for
survival by isolating them from
predatory, nonnative fish species.
Our response: We agree that existing
diversions on some streams function as
a manmade barrier and prevent the
egress of nonnative, predatory fish into
currently isolated, upstream damselfly
habitat sites. However, existing
diversions also alter the historical
amount and flow rate of water within
many lower stream sections because the
diversions either reduce the amount of
water flow at the point of diversion or
capture all stream water during times of
drier weather or drought. Therefore, the
net impact of stream diversions in the
Hawaiian Islands has been and
continues to be an overall reduction in
the amount of suitable stream habitat
available to both the Pacific Hawaiian
damselfly and the flying earwig
Hawaiian damselfly.
(8) Comment: One commenter noted
that the recently mandated interim instream flow standards (IIFS) established
by the Commission for Water Resource
Management (CWRM) for 10 east Maui
streams diverted by the East Maui
Irrigation Company (EMI) may either
benefit existing damselfly populations
or allow entry of nonnative fish species
into currently fish-isolated damselfly
habitat. The commenter further stated
that the proposed rule incorrectly
identifies the 1988 IIFS as current while
newer standards have been mandated.
Our response: We agree that the
potential release of additional water into
streams that are currently being diverted
is a complex issue, and that the outcome
may be beneficial to damselflies or may
increase the threat from nonnative
predatory fish. As of the date of
publication of this final rule, it is our
understanding that the recently
proposed IIFS have yet to be approved
and implemented by the CWRM, and we
therefore recognize the 1988 standards
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as current. Because the new standards
have not yet been implemented, we are
unable to determine their effectiveness
in enhancing damselfly habitat.
Should the proposed IIFS be
approved as the new standard, we will
strongly support a collaborative
conservation effort between our agency;
the State; the CWRM; and affected
landowners, leaseholders, and other
entities, to analyze the potential return
of water flow into currently diverted
streams on a case-by-case basis, to
ensure the protection of the Pacific
Hawaiian and the flying earwig
Hawaiian damselflies and their stream
or stream-associated habitat.
(9) Comment: One commenter
disagreed with our assessment that the
damselflies were threatened by
inadequate regulatory protections. The
commenter stated that the State Water
Code requires that the economic
benefits of stream water removal be
balanced against in-stream benefits,
including benefits to aquatic fish and
wildlife. The commenter further stated
that the CWRM’s IIFS standards provide
adequate protection for aquatic wildlife,
and the CWRM has, in the past, given
considerable deference to in-stream
benefits over stream water removal in
setting IIFS.
Our response: We believe that the
CWRM’s stated requirements to provide
protection for aquatic wildlife are
insufficiently specific to adequately
protect the damselflies or their habitat.
The CWRM’s IIFS standards do not
include provisions that address the
needs of the species. Additionally, we
lack specific examples of past CWRM
deference to in-stream benefits, and are
thus unable to determine whether
CWRM’s IIFS standards have
specifically benefited these damselflies.
(10) Comment: One commenter
explained that several of the State’s
existing hydroelectric plants do not
operate directly on streams but are
located some distance away and are
powered by water diverted from
streams.
Our response: In this final rule, we
have clarified that water is diverted to
power hydroelectric facilities regardless
of their location.
(11) Comment: One commenter noted
that some of the hydroelectric projects
identified as proposed may be
developed without diverting additional
water from streams.
Our response: We have modified the
appropriate section of this final rule to
clarify that in some cases, for some of
the State’s proposed hydroelectric
facilities, no additional water might be
diverted beyond what is currently
removed for agriculture or other
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purposes. However, the threats to the
damselflies below the point of diversion
within a given stream remain the same
due to the existing diversion, and we
believe that any additional increased
water diversion for hydroelectric power
could possibly impact damselfly
populations.
(12) Comment: One commenter noted
that water currently being diverted from
streams to generate power for some
hydroelectric projects is often returned
downstream within the same stream
system. Therefore, the potential to
impact damselfly habitat will vary
depending on location of the diversion
and location of damselfly habitat within
the respective stream system.
Our response: We have modified the
appropriate section of this final rule to
clarify that, in some streams, water
diverted for the generation of power is
returned to the same stream system.
However, the threats to the damselflies
below the point of diversion remain,
and may depend upon the difference (if
any) of the volume and quality of water
returned and the point at which the
water is returned to the stream system.
The commenter did not provide specific
examples or elaborate upon specific
streams.
(13) Comment: One commenter
clarified that the Hawaii Stream
Assessment (HSA) (CWRM 1990)
identifies 28, not 38, sites that have
potential to be developed for
hydropower. The commenter further
noted that these sites have not been
proposed for development, but rather
economically developable, and that
none of the 10 proposed sites includes
streams with Pacific Hawaiian
damselfly populations. We have added
the information regarding the proposed
hydroelectric development on the
stream site associated with the only
known location of the flying earwig
Hawaiian damselfly to our threats
analysis (see Factor A).
that the sites have been identified as
economically developable for
hydroelectric use. Populations of the
Pacific Hawaiian damselfly are located
upon three of these streams identified
only as potentially economically
developable for hydroelectric use.
Our response: We have modified the
appropriate section of this final rule to
correct the information that 28, not 38,
sites have been identified as potentially
economically developable for
hydroelectric use and that three of the
streams harboring Pacific Hawaiian
damselfly populations are not proposed
for development but rather are
identified as only potentially
developable.
(14) Comment: One commenter
observed that the HSA identifies 10 sites
where hydropower developments have
been proposed, several of which overlap
with sites identified as potentially
developable (see Comment 13). The
commenter further noted that the list of
10 sites actually proposed for
hydroelectric development does not
include streams known to be occupied
by the Pacific Hawaiian damselfly;
therefore, future hydropower
development is unlikely to impact this
species. However, one proposed site
does include the only known
population of the flying earwig
Hawaiian damselfly.
Our response: We have modified the
appropriate section of this final rule to
clarify that some of the 10 sites
proposed for development in the HSA
overlap with those sites identified as
Summary of Factors Affecting the
Species
Section 4 of the Act (16 U.S.C. 1531
et seq.) and its implementing
regulations (50 CFR part 424) set forth
the procedures for adding species to the
Federal Lists of Endangered and
Threatened Wildlife and Plants. A
species may be determined to be an
endangered or threatened species due to
one or more of the five factors described
in section 4(a)(1) of the Act. These five
listing factors are: (A) The present or
threatened destruction, modification, or
curtailment of its habitat or range; (B)
overutilization for commercial,
recreational, scientific, or educational
purposes; (C) disease or predation; (D)
the inadequacy of existing regulatory
mechanisms; and (E) other natural or
manmade factors affecting its continued
existence. Listing actions may be
warranted based on any of the above
threat factors, singly or in combination.
The threats to the flying earwig and
Pacific Hawaiian damselfly species are
summarized according to the five listing
factors in Table 1, and discussed in
detail below.
TABLE 1. SUMMARY OF THREATS TO THE FLYING EARWING HAWAIIAN DAMSELFLY AND PACIFIC
HAWAIIAN DAMSELFLY.
SPECIES
5 FACTORS
CATEGORY
THREATS
Flying Earwig
Hawaiian Damselfly
Pacific Hawaiian
Damselfly
Agriculture/urban development
X
X
Stream alteration
P
X
Habitat modification by pigs
X
—
Habitat modification by nonnative plants
X
X
Stochastic events
X
X
Climate change
P
P
FACTOR B
Overcollection
P
—
FACTOR C
Predation
A, BF (P)
A, B, F, BF
FACTOR D
Inadequate habitat protection
X
X
Inadequate protection from nonnative aquatic species
X
X
Limited populations
X
X
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FACTOR A
FACTOR E
A = ants
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B = backswimmers
F = fish
BF = bullfrogs
P = potential threat
X = known threat
Factor A. The Present or Threatened
Destruction, Modification, or
Curtailment of Its Habitat or Range
Freshwater habitats used by the flying
earwig and Pacific Hawaiian damselflies
on all of the main Hawaiian Islands are
severely altered and degraded because
of past and present land and water
management practices, including:
agriculture and urban development;
development of groundwater, perched
aquifer (aquifer sitting above main water
table), and surface water resources; and
the deliberate and accidental
introductions of nonnative animals
(Harris et al. 1993, pp. 12-13; Meier et
al. 1993, pp. 181-183).
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Habitat Destruction and Modification by
Agriculture and Urban Development
Although there has not been a
comprehensive, site-by-site assessment
of wetland loss in Hawaii (Erikson and
Puttock 2006, p. 40), Dahl (1990, p. 7)
estimated that at least 12 percent of
lowland to upper-elevation wetlands in
Hawaii had been converted to nonwetland habitat by the 1980s. If only
coastal plain (below 1,000 ft (305 m)
elevation) wetlands are considered, it is
estimated that 30 percent have been
converted for agricultural and urban
development (Kosaka l990, p. 1). These
marshlands and wetlands provided
habitat for several damselfly species,
including the Pacific Hawaiian
damselfly.
By the 1930s, water diversions had
been developed on all of the main
Hawaiian Islands, and by 1978, the
stream flow in over one-half of all of the
366 perennial streams in Hawaii had
been altered in some manner (Brasher
2003, p. 1055). All or most of the low
or average flow of the stream was, and
often still is, diverted into fields or
reservoirs, leaving many stream
channels completely dry (Takasaki et al.
1969, pp. 27-28; Harris et al. 1993, p. 12;
Wilcox 1996, p. 56). The historical
destruction and modification of habitat
continues to impact the two Hawaiian
damselflies, by restricting them to
curtailed or isolated habitat areas that
are often degraded in quality (for
example, by the presence of predatory
nonnative fishes). The present
curtailment of the habitat or range of the
flying earwig Hawaiian damselfly and
Pacific Hawaiian damselfly due to past
habitat destruction or modification in
turn limits population size, distribution,
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and connectivity, resulting in an
increased probability of local
extirpation or even extinction of the two
Hawaiian damselfly species.
Although extensive filling of
freshwater wetlands is rarely permitted
today, loss of riparian or wetland
habitats utilized by the Pacific and
flying earwig Hawaiian damselflies,
such as smaller areas of moist slopes,
emergent vegetation, and narrow strips
of freshwater seeps within anchialine
pool complexes (landlocked bodies of
water with a subterranean connection to
the ocean), still occurs. In addition,
marshes have been, and continue to be,
slowly filled and converted to meadow
habitat due to increased sedimentation
resulting from increased storm water
runoff from upslope development, the
accumulation of uncontrolled growth of
invasive vegetation, and blockage of
downslope drainage (Wilson Okamoto &
Associates, Inc. 1993, pp. 3-4 to 3-5).
The effects of future conversion of
wetland and other aquatic habitat for
agriculture and urban development are
immediate and significant for the
following reason: As noted above, an
estimated 30 percent of all coastal plain
wetlands in Hawaii have already been
lost to agriculture and urban
development, while the loss of lowland
freshwater habitat in Hawaii already
approaches 80 to 90 percent (Kosaka
1990, p. 1). Lacking the aquatic habitat
features that the damselflies require for
essential life history needs, such as
marshes, ponds, and sidepools along
streams (Pacific Hawaiian damselfly)
and riparian habitat (flying earwig
Hawaiian damselfly), these modified
areas no longer support populations of
these two Hawaiian damselflies.
Agriculture and urban development
have thus contributed to the present
curtailment of the habitat of these two
Hawaiian damselflies, and we have no
indication that this threat is likely to be
significantly ameliorated in the
foreseeable future.
Habitat Destruction and Modification by
Stream Diversion
Stream modifications began with the
early Hawaiians, who diverted water to
irrigate taro. However, unlike modern
stream diversions which often
completely dewater streams all year
around, early diversions often took no
more than half the stream flow, and
typically were periodic to occasionally
flood taro ponds at different times
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through the year, rather than
continuously flood them (Handy and
Handy 1972, pp. 58-59). The advent of
plantation sugarcane cultivation led to
far more extensive stream diversions,
with the first diversion built in 1856 on
Kauai (Wilcox 1996, p. 54). These
systems were designed to tap water at
upper elevations (above 984 ft (300 m))
by means of a concrete weir in the
stream (Wilcox 1996, p. 54). All or most
of the low or average flow of the stream
was, and often still is, diverted into
fields or reservoirs, leaving many stream
channels completely dry (Takasaki et al.
1969, pp. 27-28; Harris et al. 1993, p. 12;
Wilcox 1996, p. 56).
As noted above, by the 1930s, water
diversions had been developed on all of
the main Hawaiian Islands, and by
1978, the stream flow in over one-half
of all of the 366 perennial streams in
Hawaii had been altered in some
manner (Brasher 2003, p. 1055). Some
stream diversion systems are extensive,
such as the Waiahole Ditch, which
diverts water from 37 streams within the
range of the Pacific Hawaiian damselfly
on the windward side of Oahu to the
dry plains on the leeward side of the
island via a tunnel cut through the
Koolau mountain range (Stearns and
Vaksvik 1935, pp. 399-403). On west
Maui, as of 1978, over 49 miles (mi) (78
kilometers (km)) of stream habitat in 12
streams had been lost due to diversions,
and all of the 17 perennial streams on
west Maui are dewatered to some extent
(Maciolek 1979, p. 605). This loss of
stream habitat may have contributed to
the extirpation of the Pacific Hawaiian
damselfly population on west Maui.
Given the affiliation of the flying earwig
Hawaiian damselfly with riparian
habitats, this loss of stream habitat may
also potentially account for its absence
on west Maui. Most lower-elevation
stream segments on west Maui are now
completely dry, except during storminfluenced flows (Maciolek 1979, p.
605).
The maintenance of natural hydrology
is closely tied to the life history
requirements of the Hawaiian
damselflies, as the presence of standing
or running water is essential to
reproduction of the two species. In
addition to providing breeding habitat
for the adults, the aquatic larval stage of
the Pacific Hawaiian damselfly is
entirely dependent on water, and the
maintenance of local soil hydrology is
necessary for the persistence of uluhe
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ferns, which provide habitat for the
larval stage of the flying earwig
Hawaiian damselfly. The reduced flow
or complete dewatering of streams thus
results in the destruction or degradation
of habitat conditions for both the Pacific
and flying earwig Hawaiian damselflies.
The extensive diversion of streams on
Maui island-wide has reduced the
amount of stream habitat available to
the Pacific Hawaiian damselfly, and
potentially to the flying earwig
Hawaiian damselfly as well.
In addition to diverting water for
agriculture and domestic water supply,
streams in Hawaii have also been
diverted for use in hydroelectric power.
In some cases, the water used for power
generation is already being diverted for
another use; in other cases the water is
returned to the stream of origin. There
are a total of 18 active hydroelectric
plants operating on Hawaiian streams
on the islands of Hawaii, Kauai, and
Maui, only one of which is located on
a stream where a historical population
of the Pacific Hawaiian damselfly was
known on Kauai (Waimea). Another 28
sites have been identified as feasible for
hydroelectric development on the
islands of Hawaii, Kauai, Maui, and
Molokai (Hawaii Stream Assessment
1990, pp. xxi, 96-97). Three of the sites
identified as developable include
current populations of the Pacific
Hawaiian damselfly. A total of 10
streams have actually been proposed for
development, with some overlap
between the 28 streams identified as
feasible. Notably, the stream adjacent to
the single current remaining population
site for the flying earwig Hawaiian
damselfly on Maui is included among
those proposed for hydroelectric
development. Any additional diversion
of stream flow for use in hydroelectric
power could contribute to further loss of
stream habitat for the Pacific Hawaiian
damselfly and for the flying earwig
Hawaiian damselfly.
Habitat Modification and Destruction by
Dewatering of Aquifers
In addition to the diversion of stream
water and the resultant downstream
dewatering, many streams in Hawaii
have experienced reduced or zero
surface flow as a result of the
dewatering of their source aquifers.
Often these aquifers, which previously
fed the streams, were tapped by
tunneling or the injudicious placement
of wells (Stearns and Vaksvik 1935, pp.
386-434; Stearns 1985, pp. 291-305).
These groundwater sources were
captured for both domestic and
agricultural use and in some areas have
completely depleted nearby stream and
spring flows. For example, the Waikolu
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Stream on Molokai has reduced flow
due in part to groundwater withdrawal
(Brasher 2003, p. 1,056), which may
have reduced stream habitat available to
the Pacific Hawaiian damselfly.
Likewise, on Maui, streams in the west
Maui Mountains that flow into the
Lahaina District are fed by groundwater
leaking from breached high-elevation
dikes. Downstream of the dike
compartments, stream diversions are
designed to capture all of the low stream
flow, causing the streams downstream
to be frequently dry (U.S. Geological
Survey 2008a, p. 1), likely impacting
available habitat for the Pacific
Hawaiian damselfly, and potentially for
the flying earwig Hawaiian damselfly, in
the Honolua and Honokohau streams.
The island of Lanai lies within the
rain shadow of the west Maui
Mountains, which reach 5,788 ft (1,764
m) in elevation. Lower in elevation than
Maui, annual rainfall on Lanai’s summit
is 30 to 40 in (760 to 1,015 mm), but is
much less over the rest of the island
(University of Hawaii Department of
Geography 1998, p. 13). Flows of almost
every spring and seep on Lanai have
been diverted (Stearns 1940, pp. 73-74,
85, 88, 95). Surface waters in streams
have also been diverted by tunnels in
stream beds. Historically, Maunalei
Stream was the only perennial stream
on Lanai, and Hawaiians constructed
taro loi (ponds for cultivation of taro) in
the lower portions of this stream system.
In 1911, a tunnel was constructed at
1,100 ft (330 m) elevation that undercuts
the stream bed, diverting both the
surface and subsurface flows and
dewatering the stream from this point to
its mouth (Stearns 1940, pp. 86-88). The
Pacific Hawaiian damselfly, which
depends on stream habitat, was
historically known from Lanai but is no
longer extant on this island. The Pacific
Hawaiian damselfly was most likely
impacted by the dewatering of this
stream because it was the only
permanent stream on Lanai prior to its
dewatering. This example of the
negative impact of dewatering leads us
to conclude that dewatering poses a
threat to the Pacific Hawaiian damselfly
and the flying earwig Hawaiian
damselfly on the remaining islands
where the species persist.
Habitat Modification and Destruction by
Vertical Wells
Surface flow of streams has also been
affected by vertical wells drilled in the
past, because the basal aquifer (lowest
groundwater layer) and alluvial caprock
(sediment-deposited harder rock layer)
through which the lower sections of
streams flow can be pierced and
hydraulically connected by wells
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35997
(Stearns 1940, p. 88). This allows water
in aquifers normally feeding the stream
to be diverted elsewhere underground.
Dewatering of the streams by tunneling
and earlier, less-informed well
placement near or in streams was a
significant cause of habitat loss, and
these effects continue today.
Historically, for example, there was
sufficient surface flow in Makaha and
Nanakuli streams on Oahu to support
taro loi in their lower reaches, but this
flow disappeared subsequent to
construction of vertical wells upstream
(Devick 1995, p. 1). The inadvertent
dewatering of streams through the
piercing of their aquifers (which are
normally separated from adjacent waterbearing layers by an impermeable layer),
by tunneling or through placement of
vertical wells, caused the loss of Pacific
Hawaiian damselfly habitat, and
contributed to the Pacific Hawaiian
damselfly’s extirpation on the islands of
Oahu, Kauai, and Lanai (Polhemus and
Asquith 1996, pp. 23-24). Such
activities also reduced the extent of
stream habitat for the Pacific Hawaiian
damselfly on the islands of Maui,
Molokai, and Hawaii. Most lowerelevation stream segments on west Maui
and leeward east Maui are now
completely dry, except during storminfluenced flows (Maciolek 1979, p.
605). The flow of nearly every seep and
spring on Lanai has been captured or
bored with wells (Stearns 1940, pp. 7374, 85, 88, 95). The inadvertent drying
of streams from earlier, uninformed well
placement and other activities has
contributed to the decline of the Pacific
Hawaiian damselfly by reducing its
habitat on all of the islands from which
it was historically known. It should be
noted that the Pacific Hawaiian
damselfly was once among the most
commonly observed aquatic insects in
the islands (Howarth 1991, p. 40). The
dewatering of streams on Maui and
Hawaii may also have impacted habitat
of the flying earwig Hawaiian damselfly.
Although the State of Hawaii’s
Commission on Water Resource
Management is now more cognizant of
the effects that groundwater removal has
on streams via injudicious placement of
wells, the Commission still routinely
reviews new permit applications for
wells (Hardy 2009, p. 1). Thus, the
potential for additional well-drilling
continues to be a threat (see further
discussion under Factor D, The
Inadequacy of Existing Regulatory
Mechanisms, below), and the ongoing
effects of previously constructed vertical
wells continue to be an ongoing threat
to the Hawaiian dragonflies.
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Habitat Modification and Destruction by
Channelization
In addition to the destruction of most
of the stream habitat of the Pacific
Hawaiian damselfly and the flying
earwig Hawaiian damselfly, much of the
remaining stream habitat has been, and
continues to be, seriously degraded
throughout the Hawaiian Islands.
Stream degradation has been
particularly severe on the island of
Oahu where, by 1978, 58 percent of all
the perennial streams had been
channelized (lined, partially lined, or
altered) to control flooding (Brasher
2003, p. 1055; Polhemus and Asquith
1996, p. 24), and 89 percent of the total
length of these streams had been
channelized (Parrish et al. 1984, p. 83).
The channelization of streams creates
artificial, wide-bottomed stream beds
and often results in removal of riparian
vegetation, increased substrate
homogeneity, increased temporal water
velocity (increased water flow speed
during times of higher precipitation,
including minor and major flooding),
increased illumination, and higher
water temperatures (Parrish et al. 1984,
p. 83; Brasher 2003, p. 1052). Natural
streams meander and are lined with
rocks, trees, and natural debris, and
during times of flooding, jump their
banks. Channelized streams are
straightened and often lack natural
obstructions, and during times of higher
precipitation or flooding, facilitate a
higher water flow velocity. Hawaiian
damselflies are largely absent from
channelized portions of streams
(Polhemus and Asquith 1996, p. 24). In
contrast, undisturbed Hawaiian stream
systems exhibit a greater amount of
riffle habitat, canopy closure, higher
consistent flow velocity, and lower
water temperatures that are
characteristic of streams to which the
Hawaiian damselflies, in general, are
adapted (Brasher 2003, pp. 1054-1057).
Channelization of streams has not
been restricted to lower stream reaches.
For example, there is extensive
channelization of the Kalihi Stream, on
the island of Oahu, above 1,000-ft (300m) elevation. Extensive stream
channelization has contributed to the
extirpation of the Pacific Hawaiian
damselfly on Oahu (Englund 1999, p.
236; Polhemus 2008, pp. 45-46).
Stream diversion, channelization, and
dewatering represent significant and
immediate threats to the Pacific
Hawaiian damselfly for the following
reasons: (1) They reduce the amount
and distribution of stream habitat
available to this species; (2) they reduce
stream flow, leaving lower elevation
stream segments completely dry except
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during storms, or leaving many streams
completely dry year-round, thus
reducing or eliminating stream habitat;
and (3) they indirectly lead to an
increase in water temperature that leads
to the loss of Pacific Hawaiian damselfly
naiads due to direct physiological stress.
Because the probability of species
extinction increases when ranges are
restricted, habitat decreases, and
population numbers decline, the Pacific
Hawaiian damselfly is particularly
vulnerable to extinction due to such
changes in its stream habitats.
In addition, stream diversion,
dewatering, and vertical wells have the
potential to negatively impact, and in
some cases may have impacted, the
flying earwig Hawaiian damselfly.
Stream flow is essential to the adult
flying earwig damselfly’s breeding
requirements and is also essential to
maintaining localized soil hydrology
necessary for persistence of uluhe ferns,
which are known foraging and mating
sites for the adults and may provide
habitat for the larval stage. Should the
species’ population site stream
experience either reduced flow or
complete dewatering for an extended
period of time, it is expected that the
impact to surrounding soils and
associated vegetation, including the
uluhe ferns that are believed to be the
species’ likely larval-stage habitat, will
be soil desiccation and prolonged
vegetation dieback, respectively.
Habitat Destruction and Modification by
Feral Pigs
One of the primary threats to the
flying earwig Hawaiian damselfly is the
ongoing destruction and degradation of
its riparian habitat by nonnative
animals, particularly feral pigs (Sus
scrofa) (Polhemus and Asquith 1996, p.
22; Erickson and Puttock 2006, p. 42).
Pigs of Asian descent were first
introduced to Hawaii by the Polynesian
ancestors of Hawaiians around 400 A.D.
(Kirch 1982, pp. 3-4). Western
immigrants, beginning with Captain
Cook in 1778, repeatedly introduced
European strains (Tomich 1986, pp.
120-121). The pigs escaped
domestication and successfully invaded
all areas, including wet and mesic
forests and grasslands, on all of the
main Hawaiian Islands.
High pig densities and expansion of
their distribution have caused
indisputable widespread damage to
native vegetation on the Hawaiian
Islands (Cuddihy and Stone 1990, p.
63). Feral pigs create open areas within
forest habitat by digging up, eating, and
trampling native plant species (Stone
1985, p. 263). These open areas become
fertile ground for nonnative plant seeds
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spread through the excrement of the
pigs and by transport in their hair
(Stone 1985, p. 263). In nitrogen-poor
soils, feral pig excrement increases
nutrient availability, enhancing
establishment of nonnative weeds that
are more adapted to richer soils than are
native plants (Cuddihy and Stone 1990,
p. 65). In this manner, largely nonnative
forests replace native forest habitat
(Cuddihy and Stone 1990, p. 65). In
addition, feral pigs will root and dig for
plant tubers and worms in wetlands,
including marshes, on all of the main
Hawaiian Islands (Erikson and Puttock
2006, p. 42).
In a study conducted in the 1980s on
feral pig populations in Kipahulu Valley
on Maui, the deleterious effects of feral
pig rooting on native forest ecosystems
was documented (Diong 1982, pp. 150,
160-167). Rooting by feral pigs was
observed to be related to the search for
earthworms, with rooting depths
averaging 8 in (20 cm), and rooting was
found to greatly disrupt the leaf litter
and topsoil layers, and contribute to
erosion and changes in ground
topography. The feeding habits of pigs
were observed to create seed beds,
enabling the establishment and spread
of invasive weedy species such as
Clidemia hirta (Koster’s curse). The
study concluded that all aspects of the
feeding habits of pigs are damaging to
the structure and function of the
Hawaiian forest ecosystem (Diong 1982,
pp. 160-167).
It is likely that pigs similarly impact
the native vegetation used for perching
by adult flying earwig Hawaiian
damselflies. On Maui, feral pigs inhabit
the uluhe-dominated riparian habitat of
the flying earwig Hawaiian damselfly.
Through their rooting and digging
activities, they have significantly
degraded and destroyed the habitat of
the adult flying earwig Hawaiian
damselfly (Foote 2008, p. 1).
In addition to creating conditions that
enable the spread of nonnative plant
species, Mountainspring (1986, p. 98)
surmised that rooting by pigs depresses
insect populations that depend upon the
ground layer at some life stage or that
exhibit diel (day and night) movements.
As a result, it is likely that the presumed
habitat (seeps or damp leaf litter) of the
naiads of the flying earwig Hawaiian
damselfly is negatively impacted by
feral pig activity, including the
uprooting and denuding of native
vegetation (Foote 2008, p. 1; Polhemus
2008, p. 48).
Feral pigs are managed as a game
animal for public hunting in the more
accessible regions of the east Maui
watershed (Jokiel 2008, p. 1). This
management makes it likely that feral
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pigs will continue to exist on Maui, and
thus likely that pigs will continue to
destroy and degrade habitat of the flying
earwig Hawaiian damselfly on the
island of Maui.
The effects from introduced feral pigs
are immediate and ongoing because pigs
currently occur in the uluhe-dominated
riparian habitat of the flying earwig
Hawaiian damselfly. The threat of
habitat destruction or modification from
feral pigs is significant for the following
reasons: (1) Trampling and grazing
directly impact the vegetation used by
adult flying earwig Hawaiian
damselflies for perching and by the
terrestrial or semiterrestrial naiads; (2)
increased soil disturbance leads to
mechanical damage to plants used by
adults for perching and by the terrestrial
or semiterrestrial naiads; (3) creation of
open, disturbed areas, conducive to
weedy plant invasion and establishment
of alien plants from dispersed fruits and
seeds, results over time in the
conversion of a community dominated
by native vegetation to one dominated
by nonnative vegetation (leading to all
of the negative impacts associated with
nonnative plants, detailed below); and
(4) increased watershed erosion and
sedimentation upstream may degrade
adult breeding habitat for the flying
earwig Hawaiian damselfly. These
threats are expected to continue or
increase without control or elimination
of pig populations in these habitats.
Habitat Destruction and Modification by
Nonnative Plants
The invasion of nonnative plants,
including Clidemia hirta (Koster’s
curse), further contributes to the
degradation of Hawaii’s native forests,
including the riparian habitat of the
flying earwig Hawaiian damselfly on
Maui (Foote 2008, p. 1). Clidemia hirta
is the most serious nonnative plant
invader within the uluhe-dominated
riparian habitat where the flying earwig
Hawaiian damselfly occurs on Maui and
where it formerly occurred on the island
of Hawaii (Foote 2008, p. 1). A noxious
shrub first cultivated in Wahiawa on
Oahu before 1941, this plant is now
found on all of the main Hawaiian
Islands (Wagner et al. 1985, p. 41).
Clidemia hirta forms a dense
understory, shading out native plants
and hindering their regeneration; it is
considered a major nonnative plant
threat in wet forest areas because it
inhibits and eventually replaces native
plants (Wagner et al. 1985, p. 41; Smith
1989, p. 64). Invasive nonnatives such
as C. hirta are capable of modifying the
natural environment at the microhabitat
level by altering light availability and
soil-water regimes, and may eventually
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replace the native plant community
(Cuddihy and Stone 1990, p. 74;
Vitousek 1992, pp. 33-35). As C. hirta
can outcompete the native uluhe fern,
this invasive nonnative species poses a
threat by altering and degrading the
native plant community utilized by the
flying earwig Hawaiian damselfly.
Presently, the most significant threat
to natural ponds and marshes in Hawaii
is the nonnative species Urochloa
mutica (California grass). This
sprawling perennial grass is likely from
Africa (Erickson and Puttock 2006, p.
270). It was first noted on Oahu in 1924
and now occurs on all of the main
Hawaiian Islands (O’Connor 1999, p.
1,504), where it is considered an
aggressive invasive weed of marshes
and wetlands (Erickson and Puttock
2006, p. 270). Found from sea level to
3,610 ft (1,100 m) in elevation (Erickson
and Puttock 2006, p. 270), this plant
forms dense, monotypic stands that can
completely eliminate any open water by
layering trailing stems (Smith 1985, p.
186). Marshlands eventually convert to
meadowland when invaded by U.
mutica (Polhemus and Asquith 1996, p.
23). At Kawainui Marsh, the most
extensive marsh system remaining on
Oahu, control of U. mutica to prevent
conversion of the marsh to meadowland
is an ongoing management activity
(Wilson, Okamoto and Associates, Inc.
1993, pp. 3-4; Hawaii Ecosystems at
Risk (HEAR) 2008, p. 1). The preferred
habitat of the Pacific Hawaiian
damselfly (primarily lowland, stagnant
water, large ponds, and small pools) on
all of the Hawaiian Islands has likely
declined and continues to decline due
to the spread of U. mutica (Polhemus
and Asquith 1996, p. 23).
In conclusion, nonnative plants
represent a significant and immediate
and ongoing threat to the flying earwig
Hawaiian damselfly through habitat
destruction and modification for the
following reasons: (1) They adversely
impact microhabitat by modifying the
availability of light; (2) they alter soilwater regimes; (3) they modify nutrient
cycling processes; and (4) they
outcompete, and possibly directly
inhibit the growth of, native plant
species; ultimately, native-dominated
plant communities are converted to
nonnative plant communities (Cuddihy
and Stone 1990, p. 74; Vitousek 1992,
pp. 33-35). This conversion negatively
impacts and threatens the flying earwig
Hawaiian damselfly, which depends
upon native plant species, particularly
uluhe, for essential life history needs. In
addition, conversion of habitat from
marshlands to meadowlands caused by
the encroachment of the nonnative
Urochloa mutica threatens the Pacific
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Hawaiian damselfly. These threats are
expected to continue or increase
without control or elimination of
invasive nonnative plants in these
habitats.
Habitat Destruction and Modification by
Hurricanes, Landslides, and Drought
Stochastic (random, naturally
occurring) events, such as hurricanes,
landslides, and drought, alter or degrade
the habitat of Hawaiian damselflies
directly by modifying and destroying
native riparian, wetland, and stream
habitats (e.g., rocks and debris falling in
a stream, by mechanical damage to
riparian and wetland vegetation), and by
indirectly by creating disturbed areas
conducive to invasion by nonnative
plants that outcompete the native plants
used by damselflies for perching. We
presume these events also alter
microclimatic conditions (e.g., opening
the tree canopy, leading to an increase
in streamwater temperature; increasing
stream sedimentation) so that the
habitat no longer supports damselfly
populations. Both the flying earwig
Hawaiian damselfly and the Pacific
Hawaiian damselfly may also be
affected by temporary habitat loss (e.g.,
desiccation of streams, die-off of uluhe)
associated with droughts, which are not
uncommon on the Hawaiian Islands.
With populations that have already been
severely reduced in both abundance and
geographic distribution, and particularly
in the case of the flying earwig
Hawaiian damselfly, with only one
known population, even such a
temporary loss of habitat can have a
severe negative impact on the species.
Natural disasters such as hurricanes
and drought, and local, random
environmental events (such as
landslides), represent a significant
threat to native riparian, wetland, and
stream habitat and the two damselfly
species addressed in this final rule.
These types of events are known to
cause significant habitat damage
(Polhemus 1993, p. 86). Because the two
species addressed in this final rule now
persist in low numbers or occur in
restricted ranges, they are more
vulnerable to these events and less
resilient to such habitat disturbances.
Hurricanes, drought, and landslides,
even though unpredictable as to exact
timing, have been and are expected to
continue to be threats to the Hawaiian
damselflies. Therefore, they pose
immediate and ongoing threats to the
two damselfly species and their habitat.
Habitat Destruction and Modification by
Climate Change
Currently available information on
global climate change is not sufficiently
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precise to predict detailed changes in
the habitats and ecosystems upon which
these species rely. Consequently, the
exact nature of the impacts of climate
change on the aquatic and riparian
habitats of the flying earwig Hawaiian
damselfly and the Pacific Hawaiian
damselfly, are unknown. However,
increasing temperatures and altered
patterns of precipitation may affect
aquatic habitats through reduced stream
flow, evaporation of standing water,
increased streamwater temperature, and
the loss of native riparian and wetland
plants that comprise the habitat in
which these two species occur (Pounds
et al. 1999, pp. 611-612; Still et al. 1999,
p. 610; Benning et al. 2002, pp. 14,246
and 14,248).
Oki (2004, p. 4) noted long-term
evidence of decreased precipitation and
stream flow in the Hawaiian Islands,
based upon evidence collected by
stream gauging stations. This long-term
drying trend, coupled with existing
˜
ditch diversions and periodic El Nino–
caused drying events, has created a
pattern of severe and persistent stream
dewatering events (Polhemus 2008, p.
52). Future changes in precipitation and
the forecast of those changes are highly
uncertain because they depend, in part,
˜
˜
on how the El Nino–La Nina weather
cycle (a disruption of the ocean
atmospheric system in the tropical
Pacific having important global
consequences for weather and climate)
might change (Hawaii Climate Change
Action Plan 1998, pp. 2-10).
The flying earwig Hawaiian damselfly
and the Pacific Hawaiian damselfly may
be especially vulnerable to extinction
due to anticipated environmental
change that may result from global
climate change. Environmental changes
that may affect these species are
expected to include habitat loss or
alteration and changes in disturbance
regimes (e.g., storms and hurricanes), in
addition to direct physiological stress
caused by increased streamwater
temperatures to which the native
Hawaiian damselfly fauna are not
adapted. The probability of a species
going extinct as a result of these factors
increases when its range is restricted,
habitat decreases, and population
numbers decline (Intergovernmental
Panel on Climate Change 2007, p. 8).
Both of these damselfly species have
limited environmental tolerance ranges,
restricted habitat requirements, small
population size, and a low number of
individuals. Therefore, we would expect
these species to be particularly
vulnerable to projected environmental
impacts that may result from changes in
climate, and subsequent impacts to their
aquatic and riparian habitats (e.g.,
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Pounds et al. 1999, pp. 611-612; Still et
al. 1999, p. 610; Benning et al. 2002, pp.
14,246 and 14,248). We believe changes
in environmental conditions that may
result from climate change will likely
impact these two species and, according
to current climate projections, we do not
anticipate a reduction in this threat any
time in the near future; however, the
magnitude of this potential threat
cannot be determined at this time.
Summary of Factor A
The effects of past, present, and
potential future destruction,
modification, and degradation of native
riparian, wetland, and stream habitats
threaten the continued existence of the
flying earwig Hawaiian damselfly and
the Pacific Hawaiian damselfly, which
depend on these habitats throughout
their respective ranges. These effects
have been or continue to be caused by:
Agriculture and urban development;
stream diversion, well-drilling,
channelization, and dewatering;
introduced feral pigs; introduced plants;
and hurricanes, landslides, and drought.
The ongoing and likely increasing
effects of global climate change, while
currently unquantifiable, are also likely
to adversely impact, directly or
indirectly, the habitat of these two
species.
Agriculture and urban development,
to date, have caused the loss of 30
percent of Hawaii’s coastal plain
wetlands and 80 to 90 percent of
lowland freshwater habitat in Hawaii.
Extensive stream diversions and the
ongoing dewatering of remaining
wetland habitats continue to degrade
the quality of Pacific Hawaiian
damselfly habitat and its capability to
support viable populations of this
species and may also negatively affect
the habitat of the flying earwig
Hawaiian damselfly. Ongoing habitat
destruction and degradation caused by
feral pigs in remaining tracts of uluhedominated riparian habitat promote the
establishment and spread of nonnative
plants which, in turn, lower or destroy
the capability of the habitat to support
viable populations of the flying earwig
Hawaiian damselfly. The invasive
nonnative grass Urochloa mutica
threatens to destroy the habitat of the
Pacific Hawaiian damselfly through
conversion of marshlands to
meadowlands.
The above threats have caused the
extirpation of many flying earwig
Hawaiian damselfly and Pacific
Hawaiian damselfly populations; as a
result, their current ranges are very
restricted. The combination of restricted
range, limited habitat quantity and
quality, and low population size makes
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each of these species especially
vulnerable to extinction. Thus we
consider the present or threatened
destruction, modification, or
curtailment of the habitat and range of
the flying earwig Hawaiian damselfly
and the Pacific Hawaiian damselfly to
pose an immediate and significant
threat to these species.
Factor B. Overutilization for
Commercial, Recreational, Scientific, or
Educational Purposes
Individuals from what may be the
single remaining population of the
flying earwig Hawaiian damselfly were
collected by amateur collectors as
recently as the mid-1990s (Polhemus
2008, pp. 14-15). Although it is not
known how many individuals were
collected at that time, Polhemus (2008,
pp. 14-15) inferred that this collection
resulted in a noticeable decrease in the
population size. Furthermore, if there is
only one population of the species left,
the decreased reproduction that would
result from the removal of potential
breeding adults would have a significant
negative impact on the species.
There is a market for damselflies that
may serve as an incentive to collect
them. There are internet websites that
offer damselfly specimens or parts (e.g.,
wings) for sale. In addition, the internet
abounds with ‘‘how to’’ guides for
collecting and preserving damselfly
specimens (e.g., Abbott 2000, pp. 1-3;
van der Heijden 2005). After butterflies
and large beetles, dragonflies and
damselflies are probably the most
frequently collected insects in the world
(Polhemus 2008, pp. 14-15). A rare
specimen such as the flying earwig
Hawaiian damselfly may be particularly
attractive to potential collectors
(Polhemus 2008, pp. 14-15)). Based on
the history of collection of the flying
earwig Hawaiian damselfly, the market
for damselfly specimens or parts, and
the vulnerability of this small
population to the negative impacts of
any collection, we consider the
potential overutilization of the flying
earwig Hawaiian damselfly to pose an
immediate and significant threat to this
species.
Unlike the flying earwig Hawaiian
damselfly, which is restricted to one
remaining population site and which is
known to have previously been of
interest to odonata enthusiasts
(collectors of insects in the order
Odonata, including damselflies)
(Polhemus 2008, pp. 14-15), we do not
believe overcollection is currently a
threat to the Pacific Hawaiian damselfly,
because it is comparatively more
widespread across several population
sites on three islands and we are
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species.
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Factor C. Disease or Predation
The geographic isolation of the
Hawaiian Islands restricted the number
of original successful colonizing
arthropods and resulted in the
development of Hawaii’s unusual fauna.
Only 15 percent of the known families
of insects are represented by native
Hawaiian species (Howarth 1990, p. 11).
Some groups of insects that often
dominate continental arthropod fauna,
including social Hymenoptera (e.g., ants
and wasps), were absent during the
evolution of Hawaii’s unique arthropod
fauna. Commercial shipping and air
cargo, as well as biological
introductions to Hawaii, have resulted
in the establishment of over 3,372
species of nonnative insects (Howarth
1990, p. 18; Staples and Cowie 2001, p.
52), with an estimated continuing
establishment rate of 20 to 30 new
species per year (Beardsley 1962, p. 101;
Beardsley 1979, p. 36; Staples and
Cowie 2001, p. 52).
Nonnative arthropod predators and
parasites have also been intentionally
imported and released by individuals
and governmental agencies for
biological control of insect pests.
Between 1890 and 1985, 243 nonnative
species were introduced, sometimes
with the specific intent of reducing
populations of native Hawaiian insects
(Funasaki et al. 1988, p. 105; Lai 1988,
pp. 186-187). Nonnative arthropods,
whether purposefully or accidentally
introduced, pose a serious threat to
Hawaii’s native insects, including the
flying earwig Hawaiian damselfly and
the Pacific Hawaiian damselfly, through
direct predation (Howarth and Medeiros
1989, pp. 82-83; Howarth and Ramsay
1991, pp. 81-84; Staples and Cowie
2001, pp. 54-57).
In addition to the problems posed by
nonnative arthropods, the establishment
of various nonnative fish, frogs, and
toads that act as predators on native
Hawaiian damselflies has also had a
serious negative impact on the Pacific
Hawaiian damselfly and flying earwig
Hawaiian damselfly, as discussed
below.
Predation by Nonnative Ants
Ants are not a natural component of
Hawaii’s arthropod fauna, and the
native species of the islands evolved in
the absence of predation pressure from
ants. Ants can be particularly
destructive predators because of their
high densities, recruitment behavior,
aggressiveness, and broad range of diet
(Reimer 1993, pp. 17-18). The threat of
ant predation on the flying earwig
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Hawaiian damselfly and the Pacific
Hawaiian damselfly is amplified by the
fact that most ant species have winged
reproductive adults (Borror et al. 1989,
p. 738) and can quickly establish new
colonies in suitable habitats (Staples
and Cowie 2001, p. 55). These attributes
allow some ants to destroy otherwise
geographically isolated populations of
native arthropods (Nafus 1993, pp. 19,
22-23).
At least 47 species of ants are known
to be established in the Hawaiian
Islands (Hawaii Ants 2008, pp. 1-11),
and at least 4 particularly aggressive
species have severely impacted the
native insect fauna, likely including
native damselflies (Zimmerman 1948b,
p. 173; Reimer et al. 1990, pp. 40-43;
HEAR database 2005, pp. 1-2): The bigheaded ant (Pheidole megacephala), the
long-legged ant (also known as the
yellow crazy ant) (Anoplolepis
gracilipes), Solenopsis papuana (no
common name), and Solenopsis
geminata (no common name).
Numerous other species of ants are
recognized as threats to Hawaii’s native
invertebrates, with a trend of new
species of ants being established every
few years (Staples and Cowie 2001, pp.
53). Due to their preference for drier
habitat sites, ants are less likely to occur
in high densities in the riparian and
aquatic habitat currently occupied by
the flying earwig Hawaiian damselfly
and the Pacific Hawaiian damselfly.
However, some species of ants (e.g., the
long-legged ant and Solenopsis
papuana) have increased their range
into these areas.
The presence of ants in nearly all of
the lower elevation habitat sites
historically occupied by the flying
earwig Hawaiian damselfly and the
Pacific Hawaiian damselfly may
preclude the future recolonization of
these areas by these two species.
Damselfly naiads may be particularly
susceptible to ant predation when they
crawl out of the water or seek a
terrestrial location for their
metamorphosis into the adult stage.
Likewise, newly emerged adult
damselflies are susceptible to predation
until their wings have sufficiently
hardened to permit flight, or when the
adults are simply resting on vegetation
at night (Polhemus 2008, p. 59).
The long-legged ant appeared in
Hawaii in 1952, and now occurs on
Kauai, Oahu, Maui, and Hawaii (Reimer
et al. 1990, p. 42). It inhabits low to
mid-elevation (less than 2,000 ft (600
m)) rocky areas of moderate rainfall (less
than 100 in (250 cm) annually) (Reimer
et al. 1990, p. 42). Direct observations
indicate that Hawaiian arthropods are
susceptible to predation by this species.
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Hardy (1979, p. 34) documented the
apparent eradication of native insects
within the Kipahulu area on Maui after
this area was invaded by the long-legged
ant. Although only cursory observations
exist, long-legged ants are thought to be
a threat to populations of the Pacific
Hawaiian damselfly in mesic areas
within its elevation range due to their
particularly aggressive nature and large
colony sizes (Foote 2008, p. 1).
Solenopsis papuana is the only
abundant, aggressive ant that has
invaded intact mesic to wet forest from
sea level to over 2,000-ft (600-m)
elevation on all of the main Hawaiian
Islands, and is still expanding its range
(Reimer 1993, p. 14). Gillespie and
Reimer (1993, p. 30) found a negative
correlation between native spider
diversity and areas invaded by this ant
species. It is likely, based on our
knowledge of the expanding range of
this invasive ant, its aggressive nature,
and dense populations (Reimer 1993, p.
14), that it may threaten populations of
the Pacific Hawaiian damselfly in mesic
areas up to 2,000-ft (600-m) elevation as
well (Foote 2008, p. 1).
The rarity or disappearance of native
damselfly species, including the two
species in this final rule, from historical
observation sites over the past 100
years, is likely due to a variety of
factors. There is no documentation that
conclusively ties the decrease in
damselfly observations to the
establishment of nonnative ants in low
to montane, and mesic to wet, habitats
on the Hawaiian Islands. However, we
do have evidence that introduced ants
prey on Hawaiian damselflies. In 1998,
during a survey of an Oahu stream,
researchers observed predation by ants
upon another damselfly species, the
orangeblack Hawaiian damselfly
(Megalagrion xanthomelas) (Englund
2008, pp. 56-57). The presence of
nonnative ants in these habitats and
parallel decline of damselfly
observations in these habitats suggest
that nonnative ants may have played a
role in the decline of some populations
of the flying earwig Hawaiian damselfly
and Pacific Hawaiian damselfly.
In summary, observations and reports
have documented that ants are
particularly destructive predators
because of their high densities, broad
range of diet, and ability to establish
new colonies in otherwise
geographically isolated locations,
because the reproductive adult ants are
able to fly. Damselfly naiads are
particularly vulnerable to ant predation
when they crawl out of water or seek a
terrestrial location for metamorphosis
into adults, and newly emerged adults
are susceptible to predation until they
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can fly. In particular, the long-legged ant
and Solenopsis papuana are two
aggressive species reported from sea
level to 2,000-ft (610-m) elevation on all
of the main Hawaiian Islands. Since
their range overlaps that of both the
flying earwig and Pacific Hawaiian
damselfly species, we consider these
introduced ants to pose an immediate
and significant threat to both damselfly
species. Unless these aggressive
nonnative ant predators are eliminated
or controlled, we expect this threat to
continue or increase.
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Predation by Nonnative Backswimmers
Backswimmers, so called because
they swim upside down, are aquatic
‘‘true bugs’’ (Heteroptera).
Backswimmers are voracious predators
and frequently feed on prey much larger
than themselves, such as tadpoles, small
fish, and other aquatic insects,
including damselfly naiads (Heads
1985, p. 559; Heads 1986, p. 369).
Backswimmers are not native to Hawaii,
but several species have been
introduced. Notonecta indica (no
common name) was first collected on
Oahu in the mid-1980s and is presently
known from Oahu, Maui, and Hawaii.
Species of Notonecta are known to prey
on damselfly naiads and the mere
presence of this predator in the water
can cause naiads to reduce foraging
(which can reduce naiad growth,
development, and survival) (Heads
1985, p. 559; Heads 1986, p. 369). While
there is no documentation that
conclusively ties the decrease in
damselfly observations to the
establishment of nonnative
backswimmers in Hawaiian streams and
other aquatic habitat, the presence of
backswimmers in these habitats, the
documented predation of
backswimmers on the naiads of other
damselfly species, and the concurrent
decline of damselfly observations in
some areas suggest that these nonnative
aquatic insects may have played a role
in the decline of some damselfly
populations, including those of the
Pacific Hawaiian damselfly.
We consider predation by nonnative
backswimmers to pose a significant and
immediate threat to the Pacific
Hawaiian damselfly, because this
species has an aquatic naiad life stage.
In addition, the presence of these
predators in damselfly aquatic habitat
causes naiads to reduce foraging, which
in turn reduces their growth,
development, and survival.
Backswimmers are reported on all of the
main Hawaiian Islands except
Kahoolawe. Without elimination or
control of nonnative backswimmers, we
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expect this threat to continue or
increase over time.
Predation by Nonnative Fish
Predation by nonnative fish is a
significant threat to Hawaiian damselfly
species with aquatic life stages, such as
the Pacific Hawaiian damselfly. The
aquatic naiads tend to rest and feed near
or on the surface of the water, or on
rocks where they are exposed and
vulnerable to predation by nonnative
fish. Hawaii has only five native
freshwater fish species, comprised of
gobies (Gobiidae) and sleepers
(Eleotridae), that occur on all of the
major islands. Because these native fish
are benthic (bottom) feeders (Kido et al.
1993, pp. 43-44; Ego 1956, p. 24;
Englund 1999, pp. 236-237), Hawaii’s
stream-dwelling damselfly species
probably experienced limited natural
predation pressure due to their
avoidance of benthic areas in preference
for shallow side channels, sidepools,
and higher velocity riffles and seeps
(Englund 1999, pp. 236-237). While fish
predation has been an important factor
in the evolution of behavior in
damselfly naiads in continental systems
(Johnson 1991, pp. 8), it is speculated
that Hawaii’s stream-dwelling
damselflies adapted behaviors to avoid
the benthic feeding habits of native fish
species. Additionally, some species of
damselflies, including some of the
native Hawaiian species, are not
adapted to cohabitate with some fish
species, and are found only in bodies of
water without fish (Henrikson 1988, p.
179; McPeek 1990a, p. 83). The naiads
of the aquatic Pacific Hawaiian
damselfly tend to occupy more exposed
positions and engage in conspicuous
foraging behavior, thereby increasing
their susceptibility to fish predation
(Englund 1999, p. 232), unlike
damselflies that coevolved with
predaceous fish (Macan 1977, p. 48;
McPeek 1990b, p. 1,714). In laboratory
studies, Englund (1999, p. 232) found
that naiads of the orangeblack Hawaiian
damselfly and the Pacific Hawaiian
damselfly invariably were eaten due to
their behavior of swimming to the water
surface when exposed to two nonnative
freshwater fish. In the same study,
naiads of nonnative damselfly species
avoided predation by the same fish
species by remaining still and avoiding
surface waters (Englund 1999, p. 232).
Over 70 species of nonnative fish
have been introduced into Hawaiian
freshwater habitats (Devick 1991, p. 190;
Englund 1999, p. 226; Staples and
Cowie 2001, p. 32; Brasher 2003, p.
1,054; Englund 2004, p.27; Englund et
al. 2007, p. 232); at least 53 species are
now established in the freshwater
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habitats of Hawaii (Freshwater Fishes of
Hawaii 2008, p. 1). The initial
introduction of nonnative fish to Hawaii
began with the release of food stock
species by Asian immigrants at the turn
of the 20th century; however, the impact
of these first introductions to Hawaiian
damselflies cannot be assessed because
they predated the initial collection of
damselflies in Hawaii (Perkins 1899, pp.
64-76).
In 1905, three species of fish within
the Poeciliidae family, including the
mosquito fish (Gambusia affinis) and
the sailfin molly (Poecilia latipinna),
were introduced for biological control of
mosquitoes (Van Dine 1907, p. 9;
Englund 1999, p. 225; Brasher 2003, p.
1054). In 1922, several additional
species were introduced for mosquito
control, including the green swordtail
(Xiphophorus helleri), the moonfish
(Xiphophorus maculatus), and the
guppy (Poecilia reticulata). By 1935,
some Oahu damselfly species, including
the orangeblack Hawaiian damselfly,
were becoming less common, and fish
introduced for mosquito control were
the suspected cause of their decline
(Williams 1936, p. 313; Zimmerman
1948b, p. 341). The literature clearly
indicates that the extirpation of the
Pacific Hawaiian damselfly from the
majority of its historical habitat sites on
the main Hawaiian Islands is the result
of predation by nonnative fish (Moore
and Gagne 1982, p. 4; Liebherr and
Polhemus 1997, p. 502; Englund 1999,
pp. 235-237; Brasher 2003, p. 1,055;
Englund et al. 2007, p. 215; Polhemus
2007, pp. 238-239). From 1946 through
1961, several additional nonnative fish
were introduced for the purpose of
controlling nonnative aquatic plants,
and for angling (Brasher 2003, p. 1,054).
In the early 1980s, several additional
species of nonnative fish began
appearing in stream systems, likely
originating from the aquarium fish trade
(Devick 1991, p. 189; Brasher 2003, p.
1,054). By 1990, there were an
additional 14 species of nonnative fish
established in waters on Hawaii, Maui,
and Molokai. By 2008, there were at
least 17 nonnative freshwater fish
established on one or more of these
islands, including several aggressive
predators and habitat-altering species
such as the channel catfish (Ictalurus
punctatus) and cichlids (Tilapia sp.)
(Devick 1991, pp. 191-192; FishBase
2008).
The Pacific Hawaiian damselfly is
currently found only in portions of
stream systems without nonnative fish
(Liebherr and Polhemus 1997, pp. 493494; Englund 1999, p. 228; Englund
2004, p. 27; Englund et al. 2007, p. 215).
There is a strong correlation between
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the absence of nonnative fish species
and the presence of Hawaiian
damselflies in streams on all of the main
Hawaiian Islands (Englund 1999, p. 225;
Englund et al. 2007, p. 215), suggesting
that the damselflies cannot coexist with
nonnative fish. The distribution of some
Hawaiian damselfly species is now
reduced to stream reaches less than 312
ft (95 m) in length where invasive fish
species do not occur (Englund 1999, p.
229; Englund 2004, p. 27). In 2007, a
Statewide survey including 15 streams
on the islands of Hawaii, Maui, and
Molokai found the flying earwig
Hawaiian damselfly was not observed in
streams where the introduced Mexican
molly (Poecilia mexicana) was present
(Englund et al. 2007, pp. 214-216, 228).
On Oahu, researchers found that the
Oahu-endemic Hawaiian damselflies
only occupied habitat sites without
nonnative fish. For two of these species,
a geologic or manmade barrier (e.g.,
waterfalls, steep gradient, dry stream
midreaches, or constructed diversions)
appears to prevent access by the
nonnative fish species. For this reason,
researchers have recommended that
geologically isolated sites inaccessible
to nonnative fishes, such as isolated
anchialine ponds, high-gradient streams
interrupted by manmade diversions,
and streams entering the coast as
waterfalls, be used as restoration sites
for damselflies on all of the Hawaiian
Islands (Englund 2004, p. 27).
Of the two damselfly species
considered in this final rule, the aquatic
Pacific Hawaiian damselfly appears to
have had the greatest range contraction
due to predation by nonnative fish
(Englund 1999, p. 235; Polhemus 2007,
p. 234, 238-240). Once found on all of
the main Hawaiian Islands, it is now
found only on Molokai, Maui, and one
stream on the island of Hawaii below
2,000 ft (600 m) in elevation; all are in
stream reaches free of nonnative fish.
The Pacific Hawaiian damselfly was
extirpated from Oahu by 1910 (Liebherr
and Polhemus 1997, p. 502), although
Englund (1999, p. 235) found that Oahu
still has abundant and otherwise
suitable lowland and coastal water
habitat to support this species.
However, this aquatic habitat is infested
with nonnative fish, with some
nonnative species occurring up to 1,300ft (400-m) elevation. In contrast,
Englund (1999, p. 236) found that even
at sea level, artificial wetlands (resulting
from taro cultivation) on the island of
Molokai can support populations of the
Pacific Hawaiian damselfly because
nonnative fish are absent.
Even the geographically isolated
stream headwaters and other aquatic
habitats where the Pacific Hawaiian
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damselfly remains extant are not secure
from the threat of predation by
introduced fish species. There are many
documented cases of people moving
nonnative fish from one area to another
(Brock 1995, pp. 3-4; Englund 1999, p.
237). Once nonnative fish species are
introduced to aquatic habitats
previously free of nonnative fish, they
often become permanently established
(Englund and Filbert 1999, p. 151;
Englund 1999, pp. 232-233; Englund et
al. 2007). An example of facilitated fish
movement occurred in 2000, when an
uninformed maintenance worker
introduced Tilapia sp. into pools
located on the grounds of Tripler
Hospital that were maintained for the
benefit of the remaining Oahu
population of the orangeblack Hawaiian
damselfly (Englund 2000).
The continued introduction and
establishment of new species of
predatory nonnative fish in Hawaiian
waters, and the possible movement of
these nonnative species to new streams
and other aquatic habitat, is an
immediate and significant threat to the
survival of the aquatic Pacific Hawaiian
damselfly. Unless nonnative predatory
fish are eradicated or effectively
controlled in the habitats utilized by the
Pacific Hawaiian damselfly, we have no
reason to believe that there will be any
significant reduction in this threat at
any time in the near future. The flying
earwig Hawaiian damselfly is not
known to be threatened by predation
from nonnative fish species, due to the
apparent absence of the larval stage
within stream habitats.
Predation by Introduced Frogs and
Toads
Currently, there are three species of
introduced aquatic amphibians known
in the Hawaiian Islands: The North
American bullfrog (Rana catesbeiana),
the cane toad (Bufo marinus), and the
Japanese wrinkled frog (Rana rugosa).
The bullfrog is native to the eastern
United States and the Great Plains
region (Moyle 1973, p. 18; Bury and
Whelan 1985 in Earlham College 2002,
p. 10), and was first introduced into
Hawaii in 1899 (Bryan 1931, p. 63) to
help control insects, specifically the
nonnative Japanese beetle (Popillia
japonica), a significant pest of
ornamental plants (Bryan 1931, p. 62).
Bullfrogs were first released and quickly
became established in the Hilo region
on the island of Hawaii (Bryan 1931, p.
63). Bullfrogs have demonstrated great
success in establishing new populations
wherever they have been introduced
(Moyle 1973, p. 19), and now occur on
the islands of Hawaii, Kauai, Lanai,
Maui, Molokai, and Oahu (U.S.
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36003
Geological Survey 2008b, p. 8). This
species is flexible in both habitat and
food requirements (Bury and Whelan
1985 in Earlham College 2002, p. 11),
and can utilize any water source within
its temperature range (60 to 75 degrees
Fahrenheit (°F)) (16 to 24 degrees
Celsius (°C)) (DesertUSA 2008).
Introduced to areas outside its native
range, the bullfrog’s primary impact is
typically the elimination of native frog
species (Moyle 1973, p. 21). In Hawaii,
where there are no native frogs, the
bullfrog has not been definitively
implicated in the extirpation of any
particular native aquatic invertebrate
species, but Englund et al. (2007, pp.
215, 219) found a strong correlation
between the presence of bullfrogs and
the absence of Hawaiian damselflies in
their 2006 study of streams on all of the
main Hawaiian Islands. As the bullfrog
prefers habitats with dense vegetation
and relatively calm water (Moyle 1973,
p. 19; Bury and Whelan 1985 in
Earlham College 2002, p. 9), it is likely
of particular threat to the Pacific
Hawaiian damselfly because this species
also prefers calm water habitat that is
surrounded by dense vegetation.
Capable of breeding within small pools
of water, bullfrogs are also a potential
threat to the flying earwig Hawaiian
damselfly within its uluhe-covered,
steep, riparian, and moist talus-slope
habitat on Maui.
Because the effects of possible
predation by the cane toad and the
Japanese wrinkled frog on the flying
earwig Hawaiian damselfly and the
Pacific Hawaiian damselfly are
unknown at this time, the magnitude or
significance of this potential threat
cannot be determined.
We consider predation by bullfrogs to
pose a significant and immediate threat
to the Pacific Hawaiian damselfly, since
Englund et al. (2007, pp. 215, 219)
found a strong correlation between the
presence of predatory nonnative
bullfrogs and the absence of Hawaiian
damselflies, and the preferred habitat of
the bullfrog overlaps with that of the
Pacific Hawaiian damselfly. Within its
riparian habitat, the flying earwig
Hawaiian damselfly may also be
threatened by the bullfrog, which is
capable of breeding within small pools
of water. In the absence of the
elimination or control of nonnative
bullfrogs, we expect that this threat will
continue or increase in the future.
Summary of Factor C
Predation by nonnative animal
species (ants, backswimmers, fish, and
bullfrogs) poses an immediate and
significant threat to the Pacific and
flying earwig Hawaiian damselflies
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throughout their ranges for the
following reasons:
• Damselfly naiads are vulnerable to
predation by ants, and the ranges of
both the Pacific and flying earwig
Hawaiian damselflies overlap that
of particularly aggressive,
nonnative, predatory ant species
that currently occur from sea level
to 2,000 ft (610 m) elevation on all
of the main Hawaiian Islands. We
consider both the Pacific and flying
earwig Hawaiian damselflies to be
threatened by predation by these
nonnative ants.
• Nonnative backswimmers prey on
damselfly naiads in streams and
other aquatic habitat, and are
considered a threat to the Pacific
Hawaiian damselfly since this
species has an aquatic naiad life
stage. In addition, the presence of
backswimmers inhibits the foraging
behavior of damselfly naiads, with
negative consequences for
development and survival.
Backswimmers are reported on all
of the main Hawaiian Islands
except Kahoolawe.
• The absence of Hawaiian damselflies,
including the aquatic Pacific
Hawaiian damselfly, in streams and
other aquatic habitat on the main
Hawaiian Islands, is strongly
correlated with the presence of
predatory nonnative fish as
documented in numerous
observations and reports (Englund
1999, p. 237; Englund 2004, p. 27;
Englund et al. 2007, p. 215), thereby
suggesting that nonnative predatory
fishes eliminated native Hawaiian
damselflies from these aquatic
habitats. There are over 51 species
of nonnative fishes established in
freshwater habitats on the Hawaiian
Islands from sea level to over 3,800ft (1,152-m) elevation (Devick 1991,
p. 190; Staples and Cowie 2001, p.
32; Brasher 2003, p. 1054; Englund
1999, p. 226; Englund and
Polhemus 2001; Englund 2004, p.
27; Englund et al. 2007, p. 232).
Predation by nonnative fishes is
considered to pose a significant and
immediate threat to the Pacific
Hawaiian damselfly.
• Englund et al. (2007, pp. 215, 219)
found a strong correlation between
the presence of nonnative bullfrogs
and the absence of Hawaiian
damselflies. Bullfrogs are reported
on all of the main Hawaiian Islands,
except Kahoolawe and Niihau. The
Pacific Hawaiian damselfly is likely
threatened by bullfrogs, due to their
shared preference for similar
habitat, and the flying earwig
Hawaiian damselfly may also be
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threatened within its riparian
habitat by the bullfrog, which is
capable of breeding within small
pools of water.
Factor D. The Inadequacy of Existing
Regulatory Mechanisms
Inadequate Habitat Protection
Currently, there are no Federal, State,
or local laws, treaties, or regulations that
specifically conserve or protect the
flying earwig Hawaiian damselfly or the
Pacific Hawaiian damselfly from the
threats described in this final rule. The
State of Hawaii considers all natural
flowing surface water (streams, springs,
and seeps) as State property (Hawaii
Revised Statutes 174c 1987), and the
Hawaii Department of Land and Natural
Resources (DLNR), Division of Aquatic
Resources has management
responsibility for the aquatic organisms
in these waters (Hawaii Revised Statutes
Annotated, 1988, Title 12; 1992
Cumulative Supplement). Thus,
damselfly populations associated with
streams, seeps, and springs are under
the jurisdiction of the State of Hawaii,
regardless of the ownership of the
property across which the stream flows.
This includes all populations of the
Pacific Hawaiian damselfly and the
flying earwig Hawaiian damselfly.
The State of Hawaii manages the use
of surface and groundwater resources
through the Commission on Water
Resource Management (Water
Commission), as mandated by the 1987
State Water Code (State Water Code,
Hawaii Revised Statutes Chapter 174C71, 174C-81-87, and 174C-9195, and
Administrative Rules of the State Water
Code, Title 13, Chapters 168 and 169).
In the State Water Code, there are no
formal requirements that project
proponents or the Water Commission
protect the habitats of fish and wildlife
prior to issuance of a permit to modify
surface or groundwater resources.
As noted above in Factor A, the Water
Commission is now more cognizant of
the effects that groundwater removal has
on streams via injudicious placement of
wells. The Commission routinely
reviews new permit applications for
wells (Hardy 2009, p. 1). All requests for
new wells require a drilling permit, and,
in some cases, a use permit is
additionally required, depending upon
the intended allocation and anticipated
amount of water to be pumped from the
well. Water Management Areas have
been designated over much of Oahu and
in some areas on other neighboring
islands. Within these areas, a use permit
for a new well is also required, which
automatically triggers a greater review of
the potential impacts. Any request for a
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permit to drill a well within proximity
of streams or dike rock located at the
headwaters of streams automatically
triggers additional review (Hardy 2009).
Permits to drill wells near streams or
within dike complexes are now unlikely
to be granted because a new well would
require the amendment of in-stream
flow standards for the impacted stream.
However, such amendments are
sometimes approved. One example is
the long-contested case involving the
Waiahole Ditch on the island of Oahu
(Hawaii Department of Agriculture
2002, p. 3). In that case, the Commission
supports the removal of several million
gallons of water daily from windward
Oahu streams (Hawaii Department of
Agriculture 2002). Although a
regulatory process is in place that can
potentially address the effects of new
requests for groundwater removal on
streams, this process includes
provisions for amendments that would
result in adverse effects to groundwater
that supports streamside habitat for the
Pacific Hawaiian damselfly, and
potentially for the flying earwig
Hawaiian damselfly.
The maintenance of instream flow,
which is needed to protect the habitat
of damselflies and other aquatic
wildlife, is regulated by the
establishment of standards on a streamby-stream basis (State Water Code,
Hawaii Revised Statutes Chapter 174C71, and Administrative Rules of the
State Water Code, Title 13, Chapter
169). Currently, the interim instream
flow standards represent the existing
flow conditions in streams in the State
(as of June 15, 1988, for Molokai,
Hawaii, Kauai and east Maui; and
October 19, 1988, for west Maui and
leeward Oahu) (Administrative Rules of
the State Water Code, Title 13, Chapter
169-44-49). However, the State Water
Code does not provide permanent or
minimal instream flow standards for the
protection of aquatic wildlife. Instead,
modification of instream flow standards
and stream channels can be undertaken
at any time by the Water Commission or
via public petitions to revise flow
standards or modify stream channels in
a specified stream (Administrative Rules
of the State Water Code, Title 13,
Chapter 169-36). Additionally, the
Water Commission must consider
economic benefits gained from out-ofstream water uses, but is not required to
balance these benefits against instream
benefits or impacts to aquatic fish and
wildlife. Consequently, any stabilization
of stream flow for the protection of any
native Hawaiian damselfly species
habitat is subject to modification at a
future date.
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The natural value of Hawaii’s stream
systems has been recognized under the
State of Hawaii Instream Use Protection
Program (Administrative Rules of the
State Water Code, Title 13, Chapter 16920(2)). In the Hawaii Stream Assessment
Report (1990), prepared in coordination
with the National Park Service, the State
Water Commission identified highquality rivers or streams, or portions of
rivers or streams, that may be placed
within the Federal Wild and Scenic
River system. This report recommended
that streams meeting certain criteria be
protected from further development.
However, there is no formal or
institutional mechanism within the
State’s Water Code to designate and set
aside these streams, or to identify and
protect stream habitat for Hawaiian
damselflies. Furthermore, the setting of
instream flow standards sufficient to
conserve Hawaiian damselflies is
currently not a condition that would be
considered or included in a Hawaii
Department of Agriculture individual
permit (DLNR, Commission on Water
Resource Management 2006, p. 2).
Existing Federal regulatory
mechanisms that may protect Hawaiian
damselflies and their habitat are also
inadequate. The Federal Energy
Regulatory Commission (FERC) has very
limited jurisdiction in Hawaii. Hawaii’s
streams are isolated on individual
islands and run quickly down steep
volcanic slopes. There are no interstate
rivers in Hawaii, few if any streams
crossing Federal land, and no Federal
dams. Many of Hawaii’s streams are
generally intermittent, or if perennial,
not navigable. Thus, licensing of
hydroelectric projects in Hawaii
generally does not come under the
purview of FERC, although hydropower
developers in Hawaii may voluntarily
seek licensing under FERC.
In contrast, the U.S. Army Corps of
Engineers (Corps) has some regulatory
control over modifications of freshwater
streams in the United States, yet may
assert discretion relative to
jurisdictional determinations depending
on the surface water connection of the
stream to a tangible water of the United
States. If the Corps finds the stream to
be jurisdictional, certain activities such
as road crossings for streams and bank
stabilization can be subject to a
streamlined permitting process (33 CFR
330). This process, called the
nationwide permits program, can
involve only limited public review if
impacts are anticipated to be minimal,
both individually and cumulatively.
The Service and the Hawaii DLNR
have 15 days to provide substantive sitespecific comments prior to the issuance
of a nationwide permit. Given the
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complexity of the impacts on Hawaiian
damselflies from stream modifications
and surface water diversions, the
remoteness of project sites, and the
types of studies necessary to determine
project impacts and mitigation, this
limited comment period does not allow
time for an adequate assessment of
impacts. This regulation is inadequate
to protect the damselflies because the
Corps is under no obligation to modify
the project based upon comments
received.
However, if the stream is
jurisdictional and impacts are expected
to exceed the thresholds for a
nationwide permit, the Corps can issue
individual permits under section 404 of
the Clean Water Act (33 U.S.C. 1251 et
seq.). These permits are subject to
public review, and must comply with
the Environmental Protection Agency’s
404(b)(1) guidelines and public
comment requirements under the Clean
Water Act. Compensatory mitigation
may also be required to offset lost
stream functions. However, in issuing
these permits, the Corps does not
establish instream flow standards as a
matter of policy. The Corps normally
considers that the public interest for
instream flow is represented by the
State water allocation rights or
preferences (U.S. Army Corp of
Engineers’ Regulatory Guidance Letter
No 85-6), and project alternatives that
supersede, abrogate, or otherwise impair
the State water quantity allocations are
not normally addressed as alternatives
during permit review.
In cases where the Corps district
engineer does propose to impose
instream flow standards on an
individual permit, this flow standard
must reflect a substantial national
interest. Additionally, if this instream
flow standard is in conflict with a State
water quantity allocation, then it must
be reviewed and approved by the Office
of the Chief Engineer in Washington,
D.C. (Regulatory Guidance Letter No 856).
One population of the Pacific
Hawaiian damselfly occurs in Palikea
Stream on Maui, which flows through
Haleakala National Park. On Molokai,
populations of this damselfly species
occur at the mouth of Pelekunu Stream,
which flows through a preserve
managed by The Nature Conservancy,
and in lower Waikolu Stream, which
flows through Kalaupapa National
Historic Park. However, the landowners
do not own the water rights to any of the
streams, and thus cannot fully manage
the conservation of any of these
damselfly populations.
Because there are currently no
Federal, State, or local laws or treaties
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or regulations that adequately conserve
or protect habitat of the flying earwig
Hawaiian damselfly or the Pacific
Hawaiian damselfly from the threats
described in this final rule, and the
regulations currently in place are
inadequate to maintain stream and
riparian habitats and protect the two
damselfly species from stream
modifications and surface water
diversions, all of these threats remain
immediate and significant. The habitat
of both species continues to be reduced,
degraded, and altered by past and
present manmade alterations to streams
and riparian zones.
Inadequate Protection from Introduction
of Nonnative Species
As discussed above (see Factor C.
Disease or Predation), predation by
nonnative species (fish, insects, and
bullfrogs) is one of the most significant
threats to the survival of the flying
earwig Hawaiian damselfly and the
Pacific Hawaiian damselfly.
Based on historical and current rates
of aquatic species introductions (both
purposeful and accidental), existing
State and Federal regulatory
mechanisms are not adequately
preventing the spread of nonnative
species between islands and watersheds
in Hawaii. The Hawaii Department of
Agriculture has administrative rules in
place that address importation of
nonnative species and establish a permit
process for such activities (Hawaii
Administrative Rules sec. 4-71). The
Division of Aquatic Resources within
the Hawaii Department of Land and
Natural Resources (HDLNR) has
authority to seize, confiscate, or destroy
as a public nuisance, any fish or other
aquatic life found in any waters of the
State and whose importation is
prohibited or restricted under rules of
the Department of Agriculture (Section
187A-2(4 H.R.S. sec. 187A-6.5)).
Although State and Federal regulations
are now firmly in place to prevent the
unauthorized entry of nonnative aquatic
species into the State of Hawaii,
movement of species between islands
and from one watershed to the next
remains problematic even while
prohibited (HDAR 2003, pp. 2/12 – 2/
14). For example, while unauthorized
movement of an aquatic species from
one watershed to the next may be
prohibited, there simply is not enough
government funding to adequately
enforce such regulation or to provide for
sufficient inspection services and
monitoring, although this priority need
is recognized (Cravalho 2009, p. 1).
Furthermore, due to the complexity of
the pathways of invasion by aquatic
species (i.e., intentional, inadvertent,
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and by forces of nature), many
components contributing to the problem
may be better addressed through greater
public outreach and education
(Montgomery 2009, p. 1).
On the basis of the above information,
we find that existing regulatory
mechanisms do not adequately protect
the flying earwig Hawaiian damselfly or
the Pacific Hawaiian damselfly from the
threat of established nonnative species
(particularly fish and insect species)
spreading between islands and
watersheds, where they may prey upon
or directly compete with the two
damselfly species for food and space.
Because current Federal, State, and local
laws and treaties and regulations are
inadequate to prevent the spread of
nonnative aquatic animals between
islands and watersheds, the impacts
from these introduced threats remain
immediate and significant. From
habitat-altering, nonnative plant species
to predation or competition caused by
introduced frogs, nonnative fish, and
insect species, the Pacific Hawaiian
damselfly and the flying earwig
Hawaiian damselfly are immediately
and significantly threatened by former
and new plant and animal introductions
within the damselflies’ remaining
habitat.
Summary of Factor D
The aquatic habitat of the flying
earwig and the Pacific Hawaiian
damselflies is under the jurisdiction of
the State of Hawaii, which also has
management responsibility for aquatic
organisms. However, the State Water
Code has no regulatory mechanism in
place to protect these species or their
habitat. The State Water Code does not
currently provide for permanent or
minimum instream flow standards for
the protection of aquatic ecosystems
upon which these damselfly species
depend, and does not contain a
regulatory mechanism for identifying
and protecting damselfly habitat under
a Wild and Scenic River designation.
To date, administration of the Clean
Water Act permitting program by the
U.S. Army Corps of Engineers has not
provided substantive protection of
damselfly habitat, including any
requirements for retention of adequate
instream flows.
Existing State and Federal regulatory
mechanisms are not adequately
regulating the spread of nonnative
animal species between islands and
watersheds. Predation by nonnative
animal species poses a major ongoing
threat to the flying earwig and the
Pacific Hawaiian damselflies. Because
existing regulatory mechanisms are
inadequate to maintain aquatic habitat
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historical processes responsible for
genetic divergence within a species) of
four Megalagrion species that the Pacific
Hawaiian damselfly may be more
susceptible to problems linked to low
genetic diversity compared to other
Factor E. Other Natural or Manmade
Hawaiian damselfly species. Both Maui
Factors Affecting the Species’ Continued and Molokai populations of this species
Existence
were analyzed, and results suggested
that the Pacific Hawaiian damselfly may
Small Numbers of Populations and
not disperse well across both land and
Individuals
water, which may have led to the low
Species that are endemic to single
genetic diversity observed in the two
islands or known from few, widely
populations sampled. The authors
dispersed locations are inherently more
proposed that populations of the Pacific
vulnerable to extinction than
Hawaiian damselfly be monitored and
widespread species because of the
managed to help understand the
higher risks from genetic bottlenecks,
conservation needs of this species and
random demographic fluctuations,
the threat of population bottlenecks
climate change, and localized
(Jordan et al. 2007, p. 258). This study
catastrophes such as hurricanes,
did not include an analysis of the flying
landslides, and drought (Lande 1988, p.
earwig Hawaiian damselfly. However,
1,455; Mangel and Tier 1994, p. 607;
given that this species may now be
Pimm et al. 1988, p. 757). These
reduced to a single population, the
problems are further magnified when
potential loss of genetic diversity and
populations are few and restricted to a
threat of inbreeding depression is a
limited geographic area, and the number concern for the flying earwig Hawaiian
of individuals is very small. Populations damselfly as well.
with these characteristics face an
The small number of remaining
increased likelihood of stochastic
populations of the flying earwig
extinction due to changes in
Hawaiian damselfly (now possibly
demography, the environment, genetics, reduced to a single remaining
or other factors, in a process described
population) puts this species at
as an ‘‘extinction vortex’’ by Gilpin and
significant risk of extinction from
Soul´e (1986, pp. 24-25). Small, isolated stochastic events, such as hurricanes,
populations often exhibit a reduced
landslides, or prolonged drought (Jones
level of genetic variability or genetic
et al. 1984, p. 209). For example,
depression due to inbreeding, which
Polhemus (1993, p. 87) documented the
diminishes the species’ capacity to
extirpation of a related damselfly
adapt and respond to environmental
species, Megalagrion vagabundum, from
changes, thereby lessening the
the entire Hanakapiai Stream system on
probability of long-term persistence
Kauai as a result of the impacts from
(Soul´e 1987, pp. 4-7). The problems
Hurricane Iniki in 1992. Such stochastic
associated with small population size
events thus pose the threat of immediate
and vulnerability to random
extinction of a species with a very small
demographic fluctuations or natural
and geographically restricted
catastrophes are further magnified by
distribution, as in the case of the flying
synergistic interactions with other
earwig Hawaiian damselfly.
threats, such as those discussed above
Summary of Factor E
(Factors A–C).
Historically, the two damselfly
The threat to the flying earwig and
species were more widespread, present
Pacific Hawaiian damselflies from
on several Hawaiian islands. An
limited numbers of populations and
important benefit of this greater
individuals is significant and immediate
historical range, especially the fact they for the following reasons:
were on several islands from which they • Each of these species is subject to
are now extirpated, resulted in an
potentially reduced reproductive
advantage of redundancy: Additional
vigor due to inbreeding depression,
populations separated by some distance
particularly the flying earwig
likely allowed some populations to be
Hawaiian damselfly, which is now
spared the impacts of localized or more
apparently restricted to one
discrete catastrophic events, such as
population;
• Each of these species is subject to
narrow-track hurricanes or mud slides.
reduced levels of genetic variability
However, this advantage of redundancy
that may diminish their capacity to
has been lost with the great reduction in
adapt and respond to
the damselflies’ ranges.
environmental changes, thereby
Jordan et al. (2007, p. 247) showed in
lessening the probability of their
their genetic and comparative
long-term persistence;
phylogeography analysis (study of
for the damselflies and to regulate the
spread of nonnative species, the
inadequacy of existing regulatory
mechanisms is considered to be a
significant and immediate threat.
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• The potential benefits of redundancy
resulting from the wider historical
distribution of the species, in which
some populations might survive
stochastic events that impact other
populations of the damselflies, has
been lost as a result of the extreme
reduction in the ranges of the two
species;
• As there may be only one remaining
population of the flying earwig
Hawaiian damselfly that occurs in a
relatively restricted geographic
location, a single catastrophic
event, such as a hurricane or
landslide, could result in the
extinction of the species. Likewise,
the Pacific Hawaiian damselfly,
with several small, widely
dispersed populations, would be
vulnerable to the extirpation of
remaining populations; and
• Species with few populations and a
small number of individuals, such
as the Pacific Hawaiian damselfly
and flying earwig Hawaiian
damselfly, are less resilient to
threats that might otherwise have a
relatively minor impact on a larger
population. For example, the
reduced availability of breeding
habitat or an increase in predation
of naiads, which might be absorbed
in a relatively large population,
could result in a significant
decrease in survivorship or
reproduction of a relatively small,
isolated population. The small
population size of these two species
thus magnifies the severity of the
impact of the other threats
discussed in this final rule.
Determination
We have carefully assessed the best
scientific and commercial information
available regarding the past, present,
and future threats to the flying earwig
Hawaiian damselfly and the Pacific
Hawaiian damselfly. We find that both
of these species face immediate and
significant threats throughout their
ranges:
• Both the Pacific Hawaiian damselfly
and the flying earwig Hawaiian
damselfly face threats from past,
present, and potential future
destruction, modification, and
curtailment of their habitats,
primarily from: Agriculture and
urban development; stream
diversion, well-drilling,
channelization, and dewatering;
feral pigs and nonnative plants; and
from stochastic events like
hurricanes, landslides, and drought.
The changing environmental
conditions that may result from
climate change (particularly rising
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temperatures) are also likely to
threaten these two damselfly
species (compounded because of
the two species’ small population
sizes and limited distributions),
although currently there is limited
information on the exact nature of
these impacts (see discussion under
Factor A).
• The only known population of the
flying earwig Hawaiian damselfly is
immediately and significantly
threatened by potential recreational
collection (see Factor B).
• Both the flying earwig Hawaiian
damselfly and the Pacific Hawaiian
damselfly are subject to an
immediate and significant threat of
predation by nonnative insects
(ants) and bullfrogs. The Pacific
Hawaiian damselfly is also
similarly threatened by
backswimmers and nonnative fish
(see Factor C).
• The inadequacy of existing regulatory
mechanisms (e.g., inadequate
protection of stream habitat and
inadequate protection from the
introduction of nonnative species)
poses a threat to both species of
Hawaiian damselfly, as discussed
under Factor D above.
• Both of these species face an
immediate and significant threat
from extinction due to factors
associated with small numbers of
populations and individuals as
discussed under Factor E above.
All of the above threats are
exacerbated by the inherent
vulnerability of the flying earwig
Hawaiian damselfly and the Pacific
Hawaiian damselfly to extinction from
stochastic events at any time because of
their endemism (indigenousness), small
numbers of individuals and
populations, and restricted habitats.
The Act defines an endangered
species as any species that is ‘‘in danger
of extinction throughout all or a
significant portion of its range’’ and a
threatened species as any species ‘‘that
is likely to become endangered
throughout all or a significant portion of
its range within the foreseeable future.’’
We find that each of these two species
endemic to Hawaii is presently in
danger of extinction throughout its
entire range, based on the immediacy,
severity, and scope of the threats
described above. Therefore, on the basis
of the best available scientific and
commercial information, we are listing
the flying earwig Hawaiian damselfly
and the Pacific Hawaiian damselfly as
endangered in accordance with sections
3(6) and 4(a)(1) of the Act.
Under the Act and our implementing
regulations, a species may warrant
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listing if it is endangered or threatened
throughout all or a significant portion of
its range. Each of the two endemic
damselfly species designated as
endangered in this final rule is highly
restricted in its range, and the threats to
its survival occur throughout its range
and are not restricted to any particular
significant portion of that range.
Therefore, we assessed the status of
each species throughout its entire range.
Accordingly, our assessment and final
determination apply to each species
throughout its entire range.
Available Conservation Measures
Conservation measures provided to
species listed as endangered or
threatened under the Act include
recognition, recovery actions,
requirements for Federal protection, and
prohibitions against certain activities.
Recognition through listing results in
public awareness and conservation by
Federal, State, Tribal, and local
agencies, private organizations, and
individuals. The Act encourages
cooperation with the States and requires
that recovery actions be carried out for
all listed species. The protection
required by Federal agencies, and the
prohibitions against certain activities
are discussed, in part, below.
The primary purpose of the Act is the
conservation of endangered and
threatened species and the ecosystems
upon which they depend. The ultimate
goal of such conservation efforts is the
recovery of these listed species, so that
they no longer need the protective
measures of the Act. Subsection 4(f) of
the Act requires the Service to develop
and implement recovery plans for the
conservation of endangered and
threatened species. The recovery
planning process involves the
identification of actions that are
necessary to halt or reverse the species’
decline by addressing the threats to its
survival and recovery. The goal of this
process is to restore listed species to a
point where they are secure, selfsustaining, and functioning components
of their ecosystems.
Recovery planning includes the
development of a recovery outline
shortly after a species is listed,
preparation of a draft and final recovery
plan, and revisions to the plan as
significant new information becomes
available. The recovery outline guides
the immediate implementation of urgent
recovery actions and describes the
process to be used to develop a recovery
plan. The recovery plan identifies sitespecific management actions that will
achieve recovery of the species,
measurable criteria that determine when
a species may be downlisted or delisted,
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and methods for monitoring recovery
progress. Recovery plans also establish
a framework for agencies to coordinate
their recovery efforts and provide
estimates of the cost of implementing
recovery tasks. Recovery teams
(comprised of species experts, Federal
and State agencies, nongovernment
organizations, and stakeholders) are
often established to develop recovery
plans. When completed, the recovery
outline, draft recovery plan, and the
final recovery plan will be available
from our website (https://www.fws.gov/
endangered), or from our Pacific Islands
Fish and Wildlife Office (see
ADDRESSES).
Implementation of recovery actions
generally benefits from the participation
of a broad range of partners, including
other Federal agencies, States,
nongovernmental organizations,
businesses, and private landowners.
Examples of recovery actions include
habitat restoration (e.g., restoration of
native vegetation), research, captive
propagation and reintroduction, and
outreach and education. The recovery of
many listed species cannot be
accomplished solely on Federal lands
because their range may occur primarily
or solely on non-Federal lands. To
achieve recovery of these species
requires cooperative conservation efforts
on private and State lands.
Upon listing, funding for recovery
actions will be available from a variety
of sources, including Federal budgets,
State programs, and cost-share grants for
non-Federal landowners, the academic
community, and nongovernmental
organizations. In addition, under section
6 of the Act, the State of Hawaii is
eligible for Federal funds to implement
management actions that promote the
protection and recovery of the flying
earwig Hawaiian damselfly and the
Pacific Hawaiian damselfly. Information
on our grant programs that are available
to aid species recovery can be found at:
https://www.fws.gov/grants.
Please let us know if you are
interested in participating in recovery
efforts for the flying earwig Hawaiian
damselfly and the Pacific Hawaiian
damselfly. Additionally, we invite you
to submit any new information on these
species whenever it becomes available
and any information you may have for
recovery planning purposes (see
ADDRESSES).
Section 7(a) of the Act, as amended,
requires Federal agencies to evaluate
their actions with respect to any species
that is proposed or listed as endangered
or threatened and with respect to its
critical habitat, if any is designated.
Regulations implementing this
interagency cooperation provision of the
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Act are codified at 50 CFR part 402.
Section 7(a)(2) of the Act requires
Federal agencies to ensure that activities
they authorize, fund, or carry out are not
likely to jeopardize the continued
existence of a listed species or destroy
or adversely modify its critical habitat.
If a Federal action may affect a listed
species or its critical habitat, the
responsible Federal agency must enter
into consultation with the Service.
Federal agency actions within the
species’ habitat that may require
consultation as described in the
preceding paragraph include, but are
not limited to: Army Corps of Engineers
involvement in projects, such as the
construction of roads, bridges, and
dredging projects, subject to section 404
of the Clean Water Act (33 U.S.C. 1251
et seq.) and section 10 of the Rivers and
Harbors Act of 1899 (33 U.S.C. 401 et
seq.); U.S. Environmental Protection
Agency–authorized discharges under
the National Pollutant Discharge
Elimination System (NPDES); U.S.
Department of Agriculture involvement
in the release or permitting of the
release of biological control agents
under the Federal Plant Pest Act (7
U.S.C. 150aa-150jj); military training
and related activity carried out by the
U.S. Department of Defense; and
projects by the Natural Resources
Conservation Service, National Park
Service, U.S. Fish and Wildlife Service,
Federal Highways Administration, and
the U.S. Department of Housing and
Urban Development.
The Act and its implementing
regulations set forth a series of general
prohibitions and exceptions that apply
to all endangered and threatened
wildlife. The prohibitions of section
9(a)(2) of the Act, codified at 50 CFR
17.21 for endangered wildlife, in part,
make it illegal for any person subject to
the jurisdiction of the United States to
take (includes harass, harm, pursue,
hunt, shoot, wound, kill, trap, capture,
or collect, or attempt any of these),
import, export, ship in interstate
commerce in the course of a commercial
activity, or sell or offer for sale in
interstate or foreign commerce any
listed species. It is also illegal to
possess, sell, deliver, carry, transport, or
ship any such wildlife that has been
taken illegally. Certain exceptions apply
to our agents and State conservation
agencies.
We may issue permits to carry out
otherwise-prohibited activities
involving endangered and threatened
wildlife species under certain
circumstances. Regulations governing
permits are codified at 50 CFR 17.22 for
endangered species. A permit must be
issued for the following purposes: For
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scientific purposes, to enhance the
propagation or survival of the species,
and for incidental take in connection
with otherwise lawful activities.
It is our policy, as published in the
Federal Register on July 1, 1994 (59 FR
34272), to identify to the maximum
extent practicable at the time a species
is listed, those activities that would or
would not constitute a violation of
section 9 of the Act. The intent of this
policy is to increase public awareness of
the effect of a proposed listing on
proposed and ongoing activities within
the range of species proposed for listing.
The following activities could
potentially result in a violation of
section 9 of the Act; this list is not
comprehensive:
(1) Unauthorized collecting, handling,
possessing, selling, delivering, carrying,
or transporting of the species, including
import or export across State lines and
international boundaries, except for
properly documented antique
specimens of these taxa at least 100
years old, as defined by section 10(h)(1)
of the Act;
(2) Introduction of nonnative species
that compete with or prey upon the two
damselflies, such as the introduction of
competing nonnative insects or
predatory fish to the State of Hawaii;
(3) The unauthorized release of
biological control agents that attack any
life stage of these species;
(4) Unauthorized modification of the
channel or water flow of any stream or
removal or destruction of emergent
aquatic vegetation in any body of water
in which the flying earwig Hawaiian
damselfly and the Pacific Hawaiian
damselfly are known to occur; and
(5) Unauthorized discharge of
chemicals or fill material into any
waters in which the flying earwig
Hawaiian damselfly and the Pacific
Hawaiian damselfly are known to occur.
Questions regarding whether specific
activities would constitute a violation of
section 9 of the Act should be directed
to the Pacific Islands Fish and Wildlife
Office (see ADDRESSES). Requests for
copies of the regulations concerning
listed animals and general inquiries
regarding prohibitions and permits may
be addressed to the U.S. Fish and
Wildlife Service, Endangered Species
Permits, 911 N.E. 11th Avenue,
Portland, OR 97232-4181 (telephone
503-231-2063; facsimile 503-231-6243).
Upon listing under the Act, the State
of Hawaii’s Endangered Species Act
(HRS, Sect. 195D–4(a)) is automatically
invoked, which would also prohibit take
of these species and encourage
conservation by State government
agencies. Further, the State may enter
into agreements with Federal agencies
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to administer and manage any area
required for the conservation,
management, enhancement, or
protection of endangered species (HRS,
Sect. 195D–5(c)). Funds for these
activities could be made available under
section 6 of the Act (Cooperation with
the States). Thus, the Federal protection
afforded to these species by listing them
as endangered species will be reinforced
and supplemented by protection under
State law.
Critical Habitat
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Background
Critical habitat is defined in section 3
of the Act as:
(1) The specific areas within the
geographical area occupied by the
species, at the time it is listed in
accordance with the provisions of
section 4 of the Act, on which are found
those physical or biological features
(a) Essential to the conservation of the
species; and
(b) Which may require special
management considerations or
protections; and
(2) Specific areas outside the
geographical area occupied by a species
at the time it is listed in accordance
with the provisions of section 4 of the
Act, upon a determination by the
Secretary of the Interior that such areas
are essential for the conservation of the
species.
Conservation, as defined under
section 3 of the Act, means to use and
the use of all methods and procedures
that are necessary to bring an
endangered or threatened species to the
point at which the measures provided
under the Act are no longer necessary.
Such methods and procedures include,
but are not limited to, all activities
associated with scientific resources
management such as research, census,
law enforcement, habitat acquisition
and maintenance, propagation, live
trapping, and transplantation, and, in
the extraordinary case where population
pressures within a given ecosystem
cannot be otherwise relieved, may
include regulated taking.
Critical habitat receives protection
under section 7 of the Act through the
prohibition against Federal agencies
carrying out, funding, or authorizing the
destruction or adverse modification of
critical habitat. Section 7(a)(2) of the Act
requires consultation on Federal actions
that may affect critical habitat. The
designation of critical habitat does not
affect land ownership or establish a
refuge, wilderness, reserve, preserve, or
other conservation area. Such
designation does not allow the
government or public access to private
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lands. Such designation does not
require implementation of restoration,
recovery, or enhancement measures by
the landowner. Where a landowner
seeks or requests Federal agency
funding or authorization that may affect
a listed species or critical habitat, the
consultation requirements of section
7(a)(2) of the Act would apply, but even
in the event of a destruction or adverse
modification finding, the Federal action
agency’s and landowner’s obligation is
not to restore or recover the species, but
to implement reasonable and prudent
alternatives to avoid destruction or
adverse modification of the critical
habitat.
For inclusion in a critical habitat
designation, the habitat within the
geographical area occupied by the
species at the time of listing must
contain the physical and biological
features essential to the conservation of
the species, and be included only if
those features may require special
management considerations or
protection. Critical habitat designations
identify, to the extent known using the
best scientific data available, habitat
areas that provide essential life cycle
needs of the species (i.e., areas on which
are found the primary constituent
elements (PCEs) laid out in the
appropriate quantity and spatial
arrangement for the conservation of the
species). Under the Act, we can
designate critical habitat in areas
outside the geographical area occupied
by the species at the time it is listed
only when we determine that those
areas are essential for the conservation
of the species.
Section 4 of the Act requires that we
designate critical habitat on the basis of
the best scientific and commercial data
available. Further, our Policy on
Information Standards Under the
Endangered Species Act (published in
the Federal Register on July 1, 1994 (59
FR 34271)), the Information Quality Act
(section 515 of the Treasury and General
Government Appropriations Act for
Fiscal Year 2001 (Pub. L. 106-554; H.R.
5658)), and our associated Information
Quality Guidelines issued by the
Service, provide criteria, establish
procedures, and provide guidance to
ensure that our decisions are based on
the best scientific data available. They
require our biologists, to the extent
consistent with the Act and with the use
of the best scientific data available, to
use primary and original sources of
information as the basis for
recommendations to designate critical
habitat.
When we are determining which areas
should be designated as critical habitat,
our primary source of information is
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generally the information developed
during the listing process for the
species. Additional information sources
may include the recovery plan for the
species, if available; articles in peerreviewed journals; conservation plans
developed by States and counties;
scientific status surveys and studies;
biological assessments; or other
unpublished materials and expert
opinion or personal knowledge.
Habitat is often dynamic, and species
may move from one area to another over
time. Furthermore, we recognize that
critical habitat designated at a particular
point in time may not include all of the
habitat areas that we may later
determine are necessary for the recovery
of the species. For these reasons, a
critical habitat designation does not
signal that habitat outside the
designated area is unimportant or may
not be required for recovery of the
species.
Areas that are important to the
conservation of the species, but are
outside the critical habitat designation,
will continue to be subject to
conservation actions we implement
under section 7(a)(1) of the Act. Areas
that support populations are also subject
to the regulatory protections afforded by
section 9 prohibitions and the section
7(a)(2) jeopardy standard, as determined
on the basis of the best available
scientific information at the time of the
agency action. Federally funded or
permitted projects affecting listed
species outside their designated critical
habitat areas may still result in jeopardy
findings in some cases. Similarly,
critical habitat designations made on the
basis of the best available information at
the time of designation will not control
the direction and substance of future
recovery plans, habitat conservation
plans, or other species conservation
planning efforts if new information
available at the time of these planning
efforts warrants otherwise.
Prudency Determination
Section 4(a)(3) of the Act, as
amended, and implementing regulations
(50 CFR 424.12) require that, to the
maximum extent prudent and
determinable, the Secretary designate
critical habitat at the time a species is
determined to be endangered or
threatened. Our regulations (50 CFR
424.12(a)(1)) state that designation of
critical habitat is not prudent when one
or both of the following situations exist:
(1) The species is threatened by taking
or other human activity, and
identification of critical habitat can be
expected to increase the degree of threat
to the species, or (2) such designation of
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critical habitat would not be beneficial
to the species.
In the absence of finding that the
designation of critical habitat would
increase threats to a species, if there are
any benefits to a critical habitat
designation, then we would determine
that the designation of critical habitat is
prudent. We find that the designation of
critical habitat for the two damselfly
species addressed in this rule will
benefit them by: (1) Triggering
consultation under section 7 of the Act
for Federal actions where consultation
would not otherwise occur because, for
example, the affected area has become
unoccupied by the species or the
occupancy is in question; (2) focusing
conservation efforts on the most
essential habitat features and areas; (3)
providing educational benefits about the
species to State or County governments
or private entities; and (4) preventing
people from causing inadvertent harm
to the species.
The primary regulatory effect of
critical habitat is the section 7(a)(2)
requirement that Federal agencies
refrain from taking any action that
destroys or adversely modifies critical
habitat. On the island of Maui, one
population of the Pacific Hawaiian
damselfly occurs in a stream that flows
through Haleakala National Park, and on
the island of Molokai, one population of
this species occurs in the lower section
of a stream that flows through
Kalaupapa National Historical Park. The
National Park Service regulations and
Federal laws protect native animals in
National Parks from harassment or
destruction. Nevertheless, lands that
may be designated as critical habitat in
the future for this species may be
subject to Federal actions that trigger the
section 7 consultation requirement,
such as the granting of Federal monies
for conservation projects or the need for
Federal permits for projects, such as the
construction and maintenance of
aqueducts and bridges subject to section
404 of the Clean Water Act (33 U.S.C.
1251 et seq.).
There may also be some educational
or informational benefits from the
designation of critical habitat.
Educational benefits include the
notification of landowners, land
managers, and the general public of the
importance of protecting the habitat of
these species.
Critical habitat may play a role in
protecting habitat for future
reintroductions of a species as well. For
example, although the flying earwig
Hawaiian damselfly formerly inhabited
areas that are not currently occupied by
the species, if those currently
unoccupied areas are determined to be
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essential to the survival and recovery of
the species, they may be proposed for
designation of critical habitat. This
would alert the public that these areas
are important for the future recovery of
the species, as well as invoke the
protection of these areas under section
7 of the Act with regard to any possible
Federal actions in that area.
These aspects of critical habitat
designation would potentially benefit
the conservation of both the flying
earwig Hawaiian damselfly and the
Pacific Hawaiian damselfly. Although
collection has been identified as a threat
to the flying earwig Hawaiian damselfly,
we believe that collection poses a
potential threat to this rare species
regardless of the designation of critical
habitat. Therefore, since we have
determined that the identification of
critical habitat will not increase the
degree of threats to these species and
because the designation may provide
some measure of benefit, we find that
designation of critical habitat is prudent
for both the flying earwig Hawaiian
damselfly and the Pacific Hawaiian
damselfly.
Critical Habitat Determinability
As stated above, section 4(a)(3) of the
Act requires the designation of critical
habitat concurrently with the species’
listing ‘‘to the maximum extent prudent
and determinable.’’ Our regulations at 50
CFR 424.12(a)(2) state that critical
habitat is not determinable when one or
both of the following situations exist:
(i) Information sufficient to perform
required analyses of the impacts of the
designation is lacking, or
(ii) The biological needs of the species
are not sufficiently well known to
permit identification of an area as
critical habitat.
When critical habitat is not
determinable, the Act provides for an
additional year to publish a critical
habitat designation (16 U.S.C.
1533(b)(6)(C)(ii)).
In accordance with section 3(5)(A)(i)
of the Act and regulations at 50 CFR
424.12, in determining which areas
occupied by the species at the time of
listing to designate as critical habitat,
we consider those physical and
biological features essential to the
conservation of the species that may
require special management
considerations or protection. We
consider the physical or biological
features essential to the species’
conservation to be the primary
constituent elements laid out in the
appropriate quantity and spatial
arrangement for the conservation of the
species. The primary constituent
elements include, but are not limited to:
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(1) Space for individual and
population growth, and for normal
behavior;
(2) Food, water, air, light, minerals, or
other nutritional or physiological
requirements;
(3) Cover or shelter;
(4) Sites for breeding, reproduction,
rearing (or development) of offspring;
and
(5) Habitats that are protected from
disturbance or are representative of the
historical geographical and ecological
distributions of a species.
We are currently unable to identify
the physical and biological features that
are considered essential to the
conservation of either damselfly species,
because necessary information is not
available at this time. Key features of the
life histories of these damselfly species,
such as longevity, larval stage
requirements, and fecundity, remain
unknown. The aquatic and associated
upland habitats where the populations
of the Pacific Hawaiian damselfly are
found have been modified and altered
by development and agriculture; stream
diversions, channelization, and
dewatering; and nonnative plants. In
addition, introduced ants,
backswimmers, bullfrogs, and predatory
nonnative fish have altered and
degraded the habitat for the Pacific
Hawaiian damselfly. Likewise, the
uluhe-dominated, moist talus-slope
habitats where populations of the flying
earwig Hawaiian damselfly once
occurred have been modified and
altered by agriculture; stream
diversions, channelization, and
dewatering; and the presence of feral
pigs, nonnative plants, and introduced
ants and bullfrogs. Historically, both of
these damselfly species were much
more widespread and occurred in
habitats found on several different
islands. Because over a century has
elapsed since these species were
observed in an unaltered environment,
the optimal natural conditions that
provide the biological or ecological
requisites of these species are not
known. As described above, we can
surmise that habitat degradation from a
variety of factors and predation by a
number of nonnative species has
contributed to the decline of these
species; however, we do not know the
physical or biological features that are
essential for either of the two
damselflies addressed in this final rule.
As we are unable to identify the
physical and biological features
essential to the conservation of these
species, we are unable to identify areas
that contain these features.
Although we have determined that
the designation of critical habitat is
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prudent for the flying earwig Hawaiian
damselfly and the Pacific Hawaiian
damselfly, the biological needs of these
species are not sufficiently well known
to permit identification of the physical
and biological features that may be
essential for the conservation of the
species, or those areas essential to the
conservation of the species. Therefore,
we find that critical habitat for the
flying earwig Hawaiian damselfly and
the Pacific Hawaiian damselfly is not
determinable at this time. Over the next
year, we intend to continue gathering
information regarding the essential life
history requirements of the flying
earwig Hawaiian damselfly and the
Pacific Hawaiian damselfly to facilitate
identification of essential features and
areas. We also will evaluate the needs
of the flying earwig Hawaiian damselfly
and the Pacific Hawaiian damselfly
within the ecological context of the
broader ecosystems in which they
occur, similar to the approach that we
recently used in our designation of
critical habitat for 47 species endemic to
the island of Kauai (April 13, 2010; 75
FR 18959), and will consider the utility
of using this approach for these
damselfly species as well.
Required Determinations
Paperwork Reduction Act of 1995 (44
U.S.C. 3501 et seq.)
This rule does not contain any new
collections of information that require
approval by Office of Management and
Budget (OMB) under the Paperwork
Reduction Act. This rule will not
impose recordkeeping or reporting
requirements on State or local
governments, individuals, businesses, or
organizations. An agency may not
conduct or sponsor, and a person is not
required to respond to, a collection of
information unless it displays a
currently valid OMB control number.
Authors
National Environmental Policy Act (42
U.S.C. 4321 et seq.)
Regulation Promulgation
We have determined that
environmental assessments and
environmental impact statements, as
defined under the authority of the
National Environmental Policy Act of
1969, need not be prepared in
connection with regulations adopted
under section 4(a) of the Act. We
published a notice outlining our reasons
for this determination in the Federal
Register on October 25, 1983 (48 FR
49244).
References Cited
A complete list of all references cited
in this rule is available on the Internet
at https://www.regulations.gov or upon
request from the Field Supervisor,
Pacific Islands Fish and Wildlife Office
(see ADDRESSES).
Species
Historic range
Common name
*
Scientific name
*
Vertebrate population
where endangered or
threatened
*
*
Status
The primary authors of this document
are the staff members of the Pacific
Islands Fish and Wildlife Office.
List of Subjects in 50 CFR Part 17
Endangered and threatened species,
Exports, Imports, Reporting and
recordkeeping requirements,
Transportation.
Accordingly, we amend part 17,
subchapter B of chapter I, title 50 of the
Code of Federal Regulations, as follows:
■
PART 17—[AMENDED]
1. The authority citation for part 17
continues to read as follows:
■
Authority: 16 U.S.C. 1361-1407; 16 U.S.C.
1531-1544; 16 U.S.C. 4201-4245; Pub. L. 99625, 100 Stat. 3500; unless otherwise noted.
2. Amend § 17.11(h) by adding entries
for ‘‘Damselfly, flying earwig Hawaiian’’
and ‘‘Damselfly, Pacific Hawaiian’’ in
alphabetical order under Insects to the
List of Endangered and Threatened
Wildlife to read as follows:
■
§17.11 Endangered and threatened
wildlife.
*
*
*
(h) * * *
*
*
Critical
habitat
When listed
Special
rules
*
*
*
*
*
*
*
INSECTS
*
*
*
Damselfly, flying
earwig
Hawaiian
Megalagrion
nesiotes
U.S.A. (HI)
NA
E
271
NA
NA
Damselfly,
Pacific
Hawaiian
Megalagrion
pacificum
U.S.A. (HI)
NA
E
271
NA
NA
*
*
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*
*
Federal Register / Vol. 75, No. 121 / Thursday, June 24, 2010 / Rules and Regulations
*
*
Compliance Guide are available from
the Regional Administrator, Northeast
Regional Office, NMFS, 55 Great
Republic Drive, Gloucester, MA 01930–
2276, and are also available via the
internet at https://www.nero.nmfs.gov.
FOR FURTHER INFORMATION CONTACT:
Lindsey Feldman, Fisheries
Management Specialist, phone: 978–
675–2179, fax: 978–281–9135.
SUPPLEMENTARY INFORMATION:
*
Dated: June 11, 2010
Jeffrey L. Underwood,
Acting Director, U.S. Fish and Wildlife
Service.
[FR Doc. 2010–15237 Filed 6–23– 10; 8:45 am]
BILLING CODE 4310–55–S
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
Background
50 CFR Part 648
[Docket No. 100201058–0260–02]
RIN 0648–AY50
Fisheries of the Northeastern United
States; 2010 Specifications for the
Spiny Dogfish Fishery
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AGENCY: National Marine Fisheries
Service (NMFS), National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Final rule.
SUMMARY: NMFS announces
specifications and management
measures for the spiny dogfish fishery
for the 2010 fishing year (FY) (May 1,
2010, through April 30, 2011). NMFS is
implementing a spiny dogfish quota of
15 million lb (6,803.89 mt) for FY 2010,
and maintaining the possession limit of
3,000 lb (1.36 mt). These measures are
consistent with the Spiny Dogfish
Fishery Management Plan (FMP) and
based on new biological reference
points announced by peer reviewers of
the Transboundary Resource
Assessment Committee (TRAC), which
indicated the stock is rebuilt.
DATES: Effective July 26, 2010 through
April 30, 2011.
ADDRESSES: Copies of supporting
documents used by the Mid-Atlantic
Fishery Management Council (MAFMC),
including the Environmental
Assessment (EA) and Regulatory Impact
Review (RIR)/Initial Regulatory
Flexibility Analysis (IRFA), are
available from: Richard Seagraves,
Acting Deputy Director, Mid–Atlantic
Fishery Management Council, Room
2115, Federal Building, 300 South New
Street, Dover, DE 19904–6790. The
revised EA/RIR/IRFA updated after the
announcement of new biological
reference points is also accessible via
the Internet at https://
www.nero.noaa.gov.
NMFS prepared a Final Regulatory
Flexibility Analysis (FRFA), which is
contained in the Classification section
of the preamble of this rule. Copies of
the FRFA and the Small Entity
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12:53 Jun 23, 2010
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A proposed rule for this action was
published in the Federal Register on
April 2, 2010 (75 FR 16716), with public
comment accepted through May 3, 2010.
NMFS proposed to establish a
commercial quota of 12 million lb
(5,443.11 mt), the level calculated to
achieve the fishing mortality rate (F)
that would rebuild the stock (Frebuild)
after accounting for other sources of
fishing mortality. NMFS also proposed
maintaining the possession limit of
3,000 lb (1.36 mt) for FY 2010. As noted
in the preamble to the proposed rule,
the proposed commercial quota of 12
million lb (5,443.11 mt) was consistent
with the rebuilding F level (Frebuild =
0.11) in existence at that time. As also
noted, the Transboundary Resource
Assessment Committee (TRAC)
conducted a benchmark stock
assessment for spiny dogfish in
February 2010, and planned to reexamine biological reference points. The
proposed rule explained that the FMP
provides a mechanism to allow updated
stock status determination criteria to be
used in setting final specifications.
Details about the proposed measures
were included in the preamble of the
proposed rule and are not repeated here.
The TRAC met in early February
2010, and determined that additional
analysis would be conducted by a group
of selected peer reviewers to further
define biological reference points, in
particular to determine the status of the
spiny dogfish stock for the purposes of
U.S. management.
Revised Stock Status Determination
Criteria
On April 6, 2010, the group of peer
reviewers selected by the TRAC
accepted a newly defined biomass target
of 159,288 mt, based on analysis of
information in the TRAC assessment.
The reviewers concluded that the
updated stochastic estimate of spawning
stock biomass (SSB) for 2009 (163,256
mt) exceeded the newly defined
biomass target, and that estimates of
SSB have been above the new biomass
target since 2008, consistent with a
rebuilt stock. Therefore, the spiny
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dogfish stock can be considered rebuilt
for the purposes of U.S. management. In
addition, the peer reviewers agreed on
a new fishing mortality rate target
(Ftarget) of 0.207 (previously 0.28), which
allows 1.5 pups per recruit, and a
fishing mortality rate threshold
(Fthreshold) of 0.325 (previously 0.39).
Based on the updated stock status
determination criteria, NMFS sent a
letter to the Councils that the spiny
dogfish stock is rebuilt.
The Ftarget of 0.207 could allow the
2010 quota to be specified as high as
21.5 million lb (9,752.24 mt). However,
the Mid-Atlantic and New England
Fishery Management Councils’ Joint
Spiny Dogfish Committee (Committee)
submitted a comment on the proposed
rule that supported increasing the FY
2010 commercial quota to a level that
employs a constant catch management
approach and avoids dramatic
fluctuations in annual quota levels. In
addition, there are still a number of
concerns about the spiny dogfish stock
condition. The 2009 updated stock
assessment shows evidence of strong
recruitment; however, low pup
production from 1997 through 2003 has
been implicated by survey catches of
pups and is further supported by
subsequent low survey catches of the
size categories these age classes have
grown into. As such, a decline in the
stock is expected when these small
1997–2003 year-classes recruit into the
SSB (in approximately 2015). In
addition, the current survival rate of
pups may be lower than historic levels
due to reduced maternal size and a
skewed male-to-female sex ratio in the
population. A harvest scenario of 21.6
million lb (9,797.6 mt) over the next 5
years has only a 27 percent chance of
exceeding the biomass target (1⁄2 Bmsy)
when the small year classes from years
of low pup production recruit into the
fishery.
2010 Specifications and Management
Measures
The commercial spiny dogfish quota
for FY 2010 is 15 million lb (6,803.89
mt), the level that equates to an F of
0.167 when discard mortality and
Canadian harvest estimates are
accounted for. In setting the FY 2010
commercial quota at 15 million lb
(6,803.89 mt), there is a 98–percent
chance that the stock will not decline to
the level where it would once again be
deemed overfished, and a significant
decrease in annual quota levels will not
be necessary when the small yearclasses from years of low pup
production recruit into the fishery.
As specified in the FMP, quota Period
1 (May 1 through October 31) would be
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Agencies
[Federal Register Volume 75, Number 121 (Thursday, June 24, 2010)]
[Rules and Regulations]
[Pages 35990-36012]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-15237]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF THE INTERIOR
Fish and Wildlife Service
50 CFR Part 17
[Docket No. FWS-R1-ES-2009-0036]
[MO 92210-0-0008]
RIN 1018-AV47
Endangered and Threatened Wildlife and Plants; Listing the Flying
Earwig Hawaiian Damselfly and Pacific Hawaiian Damselfly As Endangered
Throughout Their Ranges
AGENCY: Fish and Wildlife Service, Interior.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: We, the U.S. Fish and Wildlife Service (Service), determine
endangered status under the Endangered Species Act of 1973, as amended
(Act), for two species of Hawaiian damselflies, the flying earwig
Hawaiian damselfly (Megalagrion nesiotes) on the island of Maui and the
Pacific Hawaiian damselfly (M. pacificum) on the islands of Hawaii,
Maui, and Molokai. This final rule implements the Federal protections
provided by the Act for these species. We also determine that critical
habitat for these two Hawaiian damselflies is prudent, but not
determinable at this time.
DATES: This rule becomes effective July 26, 2010.
ADDRESSES: This final rule is available on the Internet at https://www.regulations.gov and https://www.fws.gov/pacificislands. Comments and
materials received, as well as supporting documentation used in the
preparation of this rule, will be available for public inspection, by
appointment, during normal business hours at: U.S. Fish and Wildlife
Service, Pacific Islands Fish and Wildlife Office, 300 Ala Moana
Boulevard, Room 3-122, Box 50088, Honolulu, HI 96850; telephone, 808-
792-9400; facsimile, 808-792-9581.
FOR FURTHER INFORMATION CONTACT: Loyal Mehrhoff, Field Supervisor,
Pacific Islands Fish and Wildlife Office (see ADDRESSES). If you use a
telecommunications device for the deaf (TDD), call the Federal
Information Relay Service (FIRS) at 800-877-8339.
SUPPLEMENTARY INFORMATION:
Background
Damselflies are insects in the order Odonata, and are close
relatives of dragonflies, which they resemble in appearance.
Damselflies, however, are slender-bodied and fold their wings parallel
to the body while at rest, which readily distinguishes them from their
dragonfly relatives, which hold their wings out perpendicular to the
body while not in flight.
The flying earwig Hawaiian damselfly and the Pacific Hawaiian
damselfly are unique, endemic insects found only in the Hawaiian
Islands. Historically found on the islands of Hawaii and Maui, the
flying earwig Hawaiian damselfly has not been seen on the island of
Hawaii for over 80 years. Currently, the species is known only from one
location on Maui. The Pacific Hawaiian damselfly was historically found
on all of the main Hawaiian Islands except Kahoolawe and Niihau.
Currently, the Pacific Hawaiian damselfly is known only from the
islands of Hawaii, Maui and Molokai.
The Hawaiian Islands are well known for several spectacular
evolutionary radiations (the rapid evolution of new species from a
single ancestral type, as a result of adaptation and divergence in
response to new ecological conditions) resulting in unique insect fauna
found nowhere else in the world. One such group, which began its
evolution perhaps as long as 10 million years ago (Jordan et al. 2003,
p. 89), is the narrow-winged Hawaiian damselfly genus Megalagrion. This
genus appears to be most closely related to species of Pseudagrion
elsewhere in the Indo-Pacific (Zimmerman 1948a, pp. 341, 345). The
Megalagrion species of the Hawaiian Islands have evolved to occupy as
many larval breeding niches (different adaptations and ecological
conditions for breeding and development of larvae, including chemical,
physical, spatial, and temporal factors) as all the rest of the world's
damselfly species combined, and in terms of the number of insular-
endemic (native to only one island) species, are exceeded only by the
radiation of damselfly species of Fiji in the Pacific (Jordan et al.
2003, p. 91).
Native Hawaiians apparently did not differentiate the various
species, but referred to the native damselflies (and dragonflies)
collectively as ``pinao,'' and to the red-colored damselflies
specifically as ``pinao ula.'' There has been no traditional European
use of a common name for species in the genus Megalagrion. In his 1994
taxonomic review of the candidate species of insects of the Hawaiian
Islands, Nishida (1994, pp. 4-7) proposed the name ``Hawaiian
damselflies'' as the common name for species in the genus Megalagrion.
Because this name reflects the restricted distribution of these insects
and is nontechnical, the common name ``Hawaiian damselflies'' is
adopted for general use here, and we use the common names flying earwig
Hawaiian damselfly and Pacific Hawaiian damselfly to identify the two
species addressed in this final rule.
The general biology of Hawaiian damselflies is typical of other
narrow-winged damselflies (Polhemus and Asquith 1996, pp. 2-7). The
males of most species are territorial, guarding areas of habitat where
females lay eggs (Moore 1983a, p. 89). During copulation, and often
while the female lays eggs, the male grasps the female behind the head
with terminal abdominal appendages to guard the female against rival
males; thus males and females are frequently seen flying in tandem.
Female damselflies lay eggs in submerged aquatic vegetation or in
mats of moss or algae on submerged rocks, and hatching occurs in about
10 days (Williams 1936, pp. 303, 306, 318; Evenhuis et al. 1995, p.
18). In most species of Hawaiian damselflies, the immature larval
stages (naiads) are aquatic, breathing through three flattened
abdominal gills, and are predaceous, feeding on small aquatic
[[Page 35991]]
invertebrates or fish (Williams 1936, p. 303). Naiads may take up to 4
months to mature (Williams 1936, p. 309), after which they crawl out of
the water onto rocks or vegetation to molt into winged adults,
typically remaining close to the aquatic habitat from which they
emerged. The Pacific Hawaiian damselfly exhibits this typical aquatic
life history.
In contrast, the naiads of a few species of Hawaiian damselflies
are terrestrial or semiterrestrial, living on wet rock faces or in damp
terrestrial conditions, inhabiting wet leaf litter or moist leaf axils
(the angled juncture of the leaf and stem) of native plants up to
several feet above ground (Zimmerman 1970, p. 33; Simon et al. 1984, p.
13; Polhemus and Asquith 1996, p. 17). The naiads of these terrestrial
and semiterrestrial species have evolved short, thick, hairy gills and
in many species are unable to swim (Polhemus and Asquith 1996, p. 75).
The flying earwig Hawaiian damselfly is believed to exhibit this
terrestrial or semiterrestrial naiad life history.
The Hawaiian damselflies are represented by 23 species and 5
subspecies, and are currently found on 6 of the Hawaiian Islands
(Kauai, Oahu, Molokai, Maui, Lanai, and Hawaii). There are more species
of Megalagrion on the geologically older islands (12 species on Kauai)
than on the geologically youngest island (8 species on Hawaii), and
there are more single-island endemic species on the older islands (10
on Kauai) than on the youngest island (none on Hawaii) (Jordan et al.
2003, p. 91). Historically, Megalagrion damselflies were among the most
common and conspicuous native Hawaiian insects. Some species commonly
inhabited water gardens in residential areas, artificial reservoirs,
and watercress farms, and were even abundant in the city of Honolulu,
as noted by early collectors of this group (Perkins 1899, p. 76;
Perkins 1913, p. clxxviii; Williams 1936, p. 304).
Beginning with the extensive stream and wetland conversion,
alteration, and modification, and degradation of native forests through
the 20th century, Hawaii's native damselflies, including the two
species that are the subject of this final listing action, experienced
a tremendous reduction in available habitat. In addition, predation by
a number of nonnative species that have been both intentionally and, in
some cases, inadvertently introduced into the Hawaiian Islands is a
significant and ongoing threat to all native Hawaiian damselflies.
Previous Federal Actions
Both the flying earwig Hawaiian damselfly and the Pacific Hawaiian
damselfly were first designated as candidate species on May 22, 1984
(49 FR 21664). Candidate species are those taxa for which the Service
has sufficient information on their biological status and threats to
propose them for listing under the Act (16 U.S.C. 1531 et seq.), but
for which the development of a listing regulation has been precluded by
other higher-priority listing activities. The flying earwig Hawaiian
damselfly was removed from the candidate list on November 21, 1991 (56
FR 58804), whereas the Pacific Hawaiian damselfly retained its status
as a candidate species. On November 15, 1994 (59 FR 58982), the flying
earwig Hawaiian damselfly was added back onto the candidate list. In
the Candidate Notice of Review (CNOR) published on February 28, 1996
(61 FR 7595), we announced a revised list of plant and animal taxa that
we regarded as candidates for possible addition to the Lists of
Threatened and Endangered Wildlife and Plants. This revision also
included a new ranking system, whereby each candidate species was
assigned a Listing Priority Number (LPN) from 1 to 12. Both the flying
earwig Hawaiian damselfly and the Pacific Hawaiian damselfly were
assigned an LPN of 2 on February 28, 1996 (61 FR 7595).
On May 4, 2004, the Center for Biological Diversity petitioned the
Secretary of the Interior to list 225 species of plants and animals
that were already candidates, including these two Hawaiian damselfly
species, as endangered or threatened under the provisions of the Act.
In our annual CNOR, dated May 11, 2005 (70 FR 24870), we retained a
listing priority number of 2 for both of these species in accordance
with our listing priority guidance published on September 21, 1983 (48
FR 43098). A listing priority number of 2 reflects threats that are
both imminent and high in magnitude, as well as the taxonomic
classification of each of these two Hawaiian damselflies as distinct
species. At the time, we determined that publication of a proposed rule
to list these species was precluded by our work on higher priority
listing actions. Since then, we have published our annual findings on
the May 4, 2004, petition (including our findings on these two
candidate species) in the CNORs dated September 12, 2006 (71 FR 53756),
December 6, 2007 (72 FR 69034), and December 10, 2008 (73 FR 75176).
In fiscal year 2007, we determined that funding was available to
initiate work on listing determinations for these two species. On July
8, 2009, we published a proposed rule to list the flying earwig
Hawaiian damselfly and the Pacific Hawaiian damselfly as endangered (74
FR 32490). We solicited data and comments from the public on the
proposed rule for 60 days, ending September 8, 2009. To allow the
public and interested parties additional time to submit comments on the
proposed rule, we reopened the comment period on November 19, 2009 (74
FR 59956), and accepted comments until December 21, 2009.
Species Information
Flying Earwig Hawaiian Damselfly
The flying earwig Hawaiian damselfly was first described from
specimens collected in the 1890s in Puna on Hawaii Island by R.C.L.
Perkins (1899, p. 72). Kennedy (1934, pp. 343-345) described what was
believed at the time to be a new species of damselfly based on
specimens from Maui; these were later determined to be synonymous with
the specimens collected by Perkins. The flying earwig Hawaiian
damselfly is a comparatively large and elongated species. The males are
blue and black in color and exhibit distinctive, greatly enlarged,
pincer-like cerci (paired appendages on the rearmost segment of the
abdomen used to clasp the female during mating). It is for the males'
elongated abdominal appendages and their resemblance to those found on
earwigs (order Dermaptera) that the species is named. Females are
predominantly brownish in color. The adults measure from 1.8 to 1.9
inches (in) (46 to 50 millimeters (mm)) in length and have a wingspan
of 1.9 to 2.1 in (50 to 53 mm). The wings of both sexes are clear
except for the tips, which are narrowly darkened along the front
margins. Naiads of this species have never been collected or found
(Polhemus and Asquith 1996, p. 69), but they are believed to be
terrestrial or semiterrestrial in habit (Kennedy 1934, p. 345; Preston
2007a).
The biology of the flying earwig Hawaiian damselfly is not well
understood, and it is unknown if this species is more likely to be
associated with standing water or flowing water (Kennedy 1934, p. 345;
Polhemus 1994, p. 40). The only confirmed population found in the last
6 years occurs along a single East Maui stream and the adjacent steep,
moist, riparian talus slope (a slope formed by an accumulation of rock
debris), which is densely covered with Dicranopteris
[[Page 35992]]
linearis (uluhe), a native fern. Adults of the flying earwig Hawaiian
damselfly have been observed to perch on vegetation and boulders, and
to fly slowly for short distances above this particular stream within
the one known remaining habitat site. When disturbed, the adults fly
downward within nearby vegetation or between rocks, rather than up and
away as is usually observed with aquatic Hawaiian damselfly species.
Although immature individuals have not been located, based on the
habitat and the behavior of the adults, it is believed that the naiads
may be terrestrial or semiterrestrial, occurring among damp leaflitter
(Kennedy 1934, p. 345) or possibly within moist soil or seeps between
boulders in suitable habitat (Preston 2007a). The highest elevation at
which this species has been recorded is 3,000 feet (ft) (914 meters
(m)), but its close association with uluhe habitat suggests that its
range may extend upward to close to 4,000 ft (1,212 m) (Foote 2007).
Historically, the flying earwig Hawaiian damselfly was known from
the islands of Hawaii and Maui. On Hawaii, it was originally known from
seven or more general localities. The species has not been seen on
Hawaii for over 80 years, although extensive surveys within apparently
suitable habitat in the Kau and Olaa areas were conducted from 1997 to
2008 (Polhemus 2008). On Maui, the flying earwig damselfly was
historically reported from five general locations on the windward side
of the island (Kennedy 1934, p. 345). Since the 1930s, however, the
flying earwig Hawaiian damselfly has only been observed in a single
area along a particular stream on the windward side of east Maui,
despite surveys from 1993 through 2008 at several of its historically
occupied sites. Although presumed extant, the last observation of the
species was in 2005 (Foote 2008); the species was not observed during
the last survey at this location in 2008. No quantitative estimate of
the size of this remaining population is available.
It is hypothesized that the flying earwig Hawaiian damselfly may
now be restricted to what is perhaps suboptimal habitat, where periodic
absences of the species due to drought may be expected and might
explain the lack of observations of the species (Foote 2007). Some
researchers also believe that overcollection of this species by
enthusiasts may have impacted some populations in the past (Polhemus
2008). It is further possible that the individuals observed in this
area are actually part of a larger population that may be located in
the extensive belt of uluhe habitat located upslope, where the habitat
is predominantly native shrubs and matted fern understory (Foote 2007;
Hawaii Biodiversity and Mapping Program (HBMP) 2006). Unsurveyed areas
containing potentially suitable habitat for this species include the
Hana coast of east Maui, and the east rift zone of Kilauea and the Kona
area on the island of Hawaii (Foote 2007).
Pacific Hawaiian Damselfly
The Pacific Hawaiian damselfly was first described by McLachlan
(1883, p. 234), based on specimens collected by R.C.L. Perkins from
streams on the islands of Lanai and Maui. This damselfly is a
relatively small, dark-colored species, with adults measuring 1.3 to
1.4 in (34 to 37 mm) in length and having a wingspan of 1.3 to 1.6 in
(33 to 42 mm). Both adult males and females are mostly black in color.
Males exhibit brick-red striping and patterns, while females exhibit
light-green striping and patterns. The only immature individuals of
this species that have been collected were early-instar (an intermoult
stage of development) individuals, and they exhibit flattened, leaf-
like gills (Polhemus and Asquith 1996, p. 83). This species is most
easily distinguished from other Hawaiian damselflies by the extremely
long lower abdominal appendages of the male, which greatly exceed the
length of the upper appendages.
Historically, the Pacific Hawaiian damselfly was known from lower
elevations (below 2,000 ft (600 m)) on all of the main Hawaiian Islands
except Kahoolawe and Niihau (Perkins 1899, p. 64). This species was
known to breed primarily in lentic (standing water) systems such as
marshes, seepage-fed pools, large ponds at higher elevations, and
small, quiet pools in gulches that have been cut off from the main
stream channel (Moore and Gagne 1982, p. 4; Polhemus and Asquith 1996,
p. 83). The Pacific Hawaiian damselfly is no longer found in most
lentic habitats in Hawaii, such as ponds and taro (Colocasia esculenta)
fields, due to predation by nonnative fish that now occur in these
systems (Moore and Gagne 1982, p. 4; Englund et al. 2007, p. 215).
Observations have confirmed that the Pacific Hawaiian damselfly is now
restricted almost exclusively to seepage-fed pools along overflow
channels in the terminal reaches of perennial streams, usually in areas
surrounded by thick vegetation (Moore and Gagne 1982, pp. 3-4; Polhemus
1994, p. 54; Englund 1999, p. 236; Englund et al. 2007, p. 216;
Polhemus 2007, p. 238). Adults usually do not stray far from the
vicinity of the breeding pools, perching on bordering vegetation and
flying only short distances when disturbed (Polhemus and Asquith 1996,
p. 83). This species is rarely seen along main stream channels, and its
ability to disperse long distances over land or water is suspected to
be poor compared to other Hawaiian damselflies (Jordan et al. 2007, p.
254).
The Pacific Hawaiian damselfly is now believed to be extirpated
from the islands of Oahu, Kauai, and Lanai (Polhemus and Asquith 1996,
p. 83). On the island of Oahu, due to its occupation of particularly
vulnerable habitat within sidepools of lowland streams, the Pacific
Hawaiian damselfly was rare by the 1890s and appears to have been
extirpated from this island by 1910 (Liebherr and Polhemus 1997, p.
494). It is unknown when the Kauai and Lanai populations of the Pacific
Hawaiian damselfly disappeared. Until 1998, it was believed that the
species was extirpated from the island of Hawaii. That year, one
population was discovered within a small stream located just above, but
isolated from, Maili Stream, which is known to be occupied by nonnative
fish (Englund 1998, pp. 15-16). On Maui and Molokai, fewer than six
populations of the Pacific Hawaiian damselfly could be located by the
1970s (Harwood 1976, pp. 251-253; Gagne 1980, pp. 119, 125; Moore and
Gagne 1982, p. 1). The conservation of this species was identified as a
priority by the International Union for the Conservation of Nature and
Natural Resources (Moore 1982, p. 209).
The Pacific Hawaiian damselfly is currently found in at least seven
streams on Molokai and may possibly be extant in other unsurveyed
streams on Molokai's northern coast that have not been invaded by
nonnative fish (Englund 2008). On the island of Maui, the species is
currently known from 14 streams. The Pacific Hawaiian damselfly is no
longer found along the entire reaches of these Maui streams, but only
in restricted areas along each stream where steep terrain prevents
access by nonnative fish, which inhabit degraded, lower stream reaches
(Polhemus and Asquith 1996, p. 13; Englund et al. 2007, p. 215). The
species is known from a single population on the island of Hawaii, last
observed in 1998.
No quantitative estimates of the size of the extant populations are
available. Howarth (1991, p. 490) described the Pacific Hawaiian
damselfly as the most common and most widespread of the native
damselfly species at the end of the 19th century, and yet a decline in
this species was observed as early as
[[Page 35993]]
1905 due to the effects of nonnative fish introduced for control of
mosquitoes.
Summary of Comments and Recommendations
In our proposed rule published on July 8, 2009 (74 FR 32490), we
requested that all interested parties submit written comments on the
proposal by September 8, 2009. We also contacted appropriate Federal
and State agencies, scientific experts and organizations, and other
interested parties and invited them to comment on the proposal.
Newspaper notices inviting general public comment were published on the
islands of Hawaii, Maui, Molokai, and Oahu. On November 19, 2009 (74 FR
59956), we reopened the comment period for an additional 30 days,
ending December 21, 2009.
We received a total of five written comments and no requests for
public hearings. Three comments were from State of Hawaii agencies and
two were from the same nongovernmental organization. We received three
comments supporting the listing of the two Hawaiian damselflies. Two
comments neither supported nor opposed the listings, and one of these
comments provided additional information on the two damselflies. We
also requested peer review from potential peer reviewers.
Peer Review Comments
In accordance with our peer review policy published on July 1, 1994
(59 FR 34270), we solicited expert opinion from seven knowledgeable
individuals with scientific expertise that included familiarity with
the two Hawaiian damselflies and their habitat, biological needs, and
threats. We received no written comments from any of the seven peer
reviewers, although several offered their opinion that the two Hawaiian
damselfly species meet the definition of an endangered species (A.
Asquith, Hawaii Sea Grant, pers. comm. 2009; F. Howarth, Bishop Museum,
pers. comm. 2009; K. Magnacca, University of Hawaii at Hilo, pers.
comm. 2009; D. Polhemus, State of Hawaii Division of Aquatic Resources,
pers. comm. 2009; D. Preston, Bishop Museum, pers. comm. 2009).
Comments from the State of Hawaii
The State of Hawaii's State Historic Preservation Division
concurred that no historic properties would be affected by the listing
of the two Hawaiian damselflies (McMahon 2009, pers. comm.). The
State's Division of Forestry and Wildlife (DOFAW) and Office of
Hawaiian Affairs supported listing the two damselflies as endangered
(Conry 2009, pers. comm.; Namu'o 2009, pers. comm.).
Public Comments
(1) Comment: One commenter stated that there appears to be little,
if any, empirical data indicating water diversions have any potential
impact on the flying earwig Hawaiian damselfly.
Our response: While we acknowledge that the larval stage of the
flying earwig Hawaiian damselfly has never been observed within stream
water, repeated observations of the adults along the stream adjacent to
its only known population site on east Maui indicate a strong
biological association of an unknown nature with flowing stream water.
This association is likely related to the species' natural history and
may include the need for sufficient space or a stream setting for
mating adults and territorial behavior of males. Additionally, the
species' larval habitat is undoubtedly dependent on localized area
hydrology. For example, should a stream experience either reduced flow
or complete dewatering for an extended period of time, it is expected
that the impact to surrounding soils and associated vegetation,
including the uluhe ferns that are believed to be the species' likely
larval-stage habitat, will be soil desiccation and concomitant
prolonged vegetation dieback, resulting in degraded habitat conditions
for the flying earwig Hawaiian damselfly.
(2) Comment: One commenter stated the reduction or modification of
water flow in a stream should not be identified as an activity that
could potentially result in violation of section 9 of the Act
pertaining to the flying earwig Hawaiian damselfly.
Our response: As discussed in the previous response (see Comment
1), we believe there is a strong association with stream water flow and
the species' life history requirements. Stream flow is likely essential
to the adult damselfly's breeding requirements and is also essential to
maintaining localized soil hydrology necessary for persistence of uluhe
ferns, which are known foraging and mating sites for the adults and may
provide habitat for the larval stage. Therefore, any permanent or
prolonged reduction or modification of stream flow in a stream utilized
by this species may result in a violation of section 9 of the Act.
(3) Comment: One commenter stated that distribution of both species
is not fully known and recommended that the Service conduct additional
surveys for both species prior to proceeding with listing.
Our response: In preparing both the proposed and final rules for
these species, we reviewed the best scientific and commercial data
available, including technical reports, published journal articles, and
numerous other documents, including unpublished reports and surveys. In
addition, we consulted with several species experts. We based our
listing determination for the flying earwig Hawaiian damselfly and the
Pacific Hawaiian damselfly on the best available information regarding
the species' current known population status, the known condition of
their habitat, and the current factors affecting the species, along
with ongoing conservation efforts, as described in the Summary of
Factors Affecting the Species (below) in this final rule. The Act
neither provides for, nor requires, additional research effort prior to
a listing decision. We acknowledge that uncertainties exist; however,
under section 4 of the Act, we must make a listing determination based
on the best scientific and commercial available at the time of our
determination.
(4) Comment: One commenter disagreed with our analysis that stream
diversions for agriculture have reduced stream habitat available to the
Pacific Hawaiian damselfly, and currently pose a threat to this
species.
Our response: Historically, the impacts of the plantation-era
sugarcane irrigation system reduced stream habitat available to this
species. The Pacific Hawaiian damselfly was once among the most
commonly observed aquatic insects in the islands (Zimmerman 1948, p.
377). Because this species breeds in lentic habitats or stream terminal
reaches, which experienced significant modification for agriculture
beginning as early as the 19th century, the Pacific Hawaiian damselfly
was extirpated from many of its historical habitat sites (Polhemus
2007, p. 236). By the 1930s, water diversions had been developed on all
of the main Hawaiian Islands, and by 1978, the stream flow in over one-
half of all of the 366 perennial streams in Hawaii had been altered in
some manner (Brasher 2003, p. 1055). All or most of the low or average
flow of the stream was, and often still is, diverted into fields or
reservoirs, leaving many stream channels completely dry (Takasaki et
al. 1969, pp. 27-28; Harris et al. 1993, p. 12; Wilcox 1996, p. 56).
With the nearly complete cessation of this industry in the Hawaiian
Islands, it is unlikely that new irrigation-related water diversion
activities will be initiated in the remaining streams that currently
provide habitat for the Pacific Hawaiian damselfly. However, most of
the historical water diversions remain in
[[Page 35994]]
place. The historical loss of stream habitat, resulting in the present
curtailment of habitat available to the Pacific Hawaiian damselfly,
combined with the threat of predation by nonnative fish in the
remaining stream habitat, continues to restrict and reduce the amount
of habitat potentially available to this species. Should some of this
water be returned to stream systems, the amount of habitat available to
this species may increase if the water return were to be implemented
carefully to prevent the spread of nonnative fish species upstream.
(5) Comment: One commenter noted the Pacific Hawaiian damselfly,
although historically known from lower elevations, is now known to have
established successfully breeding populations at higher elevations
above existing stream diversions.
Our response: Prior to the establishment of widespread stream
diversions, the Pacific Hawaiian damselfly was considered one of the
most abundant and frequently observed insects in Hawaii and was known
from all of the main Hawaiian Islands, except Kahoolawe and Niihau.
Previously known from suitable portions of many streams and water
bodies from sea level to some higher elevation sites (Zimmerman 1948,
p. 377), the Pacific Hawaiian damselfly is now extirpated from at least
18 known population sites on the islands of Hawaii, Kauai, Lanai, Oahu,
Maui, and Molokai. Diversions changed the amount and flow rate of water
within many lower stream sections, because the diversions either
reduced the amount of water flow at the point of diversion, or captured
all stream water (as they were designed to do) during times of drier
weather or drought. The Pacific Hawaiian damselfly is currently found
in approximately 22 streams on the islands of Hawaii, Maui, and
Molokai, across a variety of elevations. All known populations are
located within streams or bodies of water free of nonnative, predatory
fish. We lack sufficient information to determine whether all stream
reaches occupied by this damselfly species are now above manmade
diversions, but we know the species is largely absent from areas below
manmade diversions.
(6) Comment: One commenter stated that the current known range of
the Pacific Hawaiian damselfly appears to be broader than the species'
known range at the time it became a candidate for listing.
Our response: We acknowledged in our proposed rule that at the time
we determined we had sufficient information on file to support a
proposal to list the Pacific Hawaiian damselfly (1984), and elevated it
to candidate status, it had been extirpated from Kauai, Oahu, and
Lanai, and was also considered extirpated from the island of Hawaii.
Subsequently in 1998, a single population was discovered on an isolated
portion of a Hilo stream on the island of Hawaii. However, since then,
the Pacific Hawaiian damselfly has not been reobserved on Kauai, Lanai,
or Oahu, and remains only on Molokai and Maui, and one location on
Hawaii Island. We do not consider the discovery of a single population
on the island of Hawaii to represent a significant broadening of the
range of the species.
(7) Comment: One commenter observed that water diversions may
enhance the damselflies' chances for survival by isolating them from
predatory, nonnative fish species.
Our response: We agree that existing diversions on some streams
function as a manmade barrier and prevent the egress of nonnative,
predatory fish into currently isolated, upstream damselfly habitat
sites. However, existing diversions also alter the historical amount
and flow rate of water within many lower stream sections because the
diversions either reduce the amount of water flow at the point of
diversion or capture all stream water during times of drier weather or
drought. Therefore, the net impact of stream diversions in the Hawaiian
Islands has been and continues to be an overall reduction in the amount
of suitable stream habitat available to both the Pacific Hawaiian
damselfly and the flying earwig Hawaiian damselfly.
(8) Comment: One commenter noted that the recently mandated interim
in-stream flow standards (IIFS) established by the Commission for Water
Resource Management (CWRM) for 10 east Maui streams diverted by the
East Maui Irrigation Company (EMI) may either benefit existing
damselfly populations or allow entry of nonnative fish species into
currently fish-isolated damselfly habitat. The commenter further stated
that the proposed rule incorrectly identifies the 1988 IIFS as current
while newer standards have been mandated.
Our response: We agree that the potential release of additional
water into streams that are currently being diverted is a complex
issue, and that the outcome may be beneficial to damselflies or may
increase the threat from nonnative predatory fish. As of the date of
publication of this final rule, it is our understanding that the
recently proposed IIFS have yet to be approved and implemented by the
CWRM, and we therefore recognize the 1988 standards as current. Because
the new standards have not yet been implemented, we are unable to
determine their effectiveness in enhancing damselfly habitat.
Should the proposed IIFS be approved as the new standard, we will
strongly support a collaborative conservation effort between our
agency; the State; the CWRM; and affected landowners, leaseholders, and
other entities, to analyze the potential return of water flow into
currently diverted streams on a case-by-case basis, to ensure the
protection of the Pacific Hawaiian and the flying earwig Hawaiian
damselflies and their stream or stream-associated habitat.
(9) Comment: One commenter disagreed with our assessment that the
damselflies were threatened by inadequate regulatory protections. The
commenter stated that the State Water Code requires that the economic
benefits of stream water removal be balanced against in-stream
benefits, including benefits to aquatic fish and wildlife. The
commenter further stated that the CWRM's IIFS standards provide
adequate protection for aquatic wildlife, and the CWRM has, in the
past, given considerable deference to in-stream benefits over stream
water removal in setting IIFS.
Our response: We believe that the CWRM's stated requirements to
provide protection for aquatic wildlife are insufficiently specific to
adequately protect the damselflies or their habitat. The CWRM's IIFS
standards do not include provisions that address the needs of the
species. Additionally, we lack specific examples of past CWRM deference
to in-stream benefits, and are thus unable to determine whether CWRM's
IIFS standards have specifically benefited these damselflies.
(10) Comment: One commenter explained that several of the State's
existing hydroelectric plants do not operate directly on streams but
are located some distance away and are powered by water diverted from
streams.
Our response: In this final rule, we have clarified that water is
diverted to power hydroelectric facilities regardless of their
location.
(11) Comment: One commenter noted that some of the hydroelectric
projects identified as proposed may be developed without diverting
additional water from streams.
Our response: We have modified the appropriate section of this
final rule to clarify that in some cases, for some of the State's
proposed hydroelectric facilities, no additional water might be
diverted beyond what is currently removed for agriculture or other
[[Page 35995]]
purposes. However, the threats to the damselflies below the point of
diversion within a given stream remain the same due to the existing
diversion, and we believe that any additional increased water diversion
for hydroelectric power could possibly impact damselfly populations.
(12) Comment: One commenter noted that water currently being
diverted from streams to generate power for some hydroelectric projects
is often returned downstream within the same stream system. Therefore,
the potential to impact damselfly habitat will vary depending on
location of the diversion and location of damselfly habitat within the
respective stream system.
Our response: We have modified the appropriate section of this
final rule to clarify that, in some streams, water diverted for the
generation of power is returned to the same stream system. However, the
threats to the damselflies below the point of diversion remain, and may
depend upon the difference (if any) of the volume and quality of water
returned and the point at which the water is returned to the stream
system. The commenter did not provide specific examples or elaborate
upon specific streams.
(13) Comment: One commenter clarified that the Hawaii Stream
Assessment (HSA) (CWRM 1990) identifies 28, not 38, sites that have
potential to be developed for hydropower. The commenter further noted
that these sites have not been proposed for development, but rather
that the sites have been identified as economically developable for
hydroelectric use. Populations of the Pacific Hawaiian damselfly are
located upon three of these streams identified only as potentially
economically developable for hydroelectric use.
Our response: We have modified the appropriate section of this
final rule to correct the information that 28, not 38, sites have been
identified as potentially economically developable for hydroelectric
use and that three of the streams harboring Pacific Hawaiian damselfly
populations are not proposed for development but rather are identified
as only potentially developable.
(14) Comment: One commenter observed that the HSA identifies 10
sites where hydropower developments have been proposed, several of
which overlap with sites identified as potentially developable (see
Comment 13). The commenter further noted that the list of 10 sites
actually proposed for hydroelectric development does not include
streams known to be occupied by the Pacific Hawaiian damselfly;
therefore, future hydropower development is unlikely to impact this
species. However, one proposed site does include the only known
population of the flying earwig Hawaiian damselfly.
Our response: We have modified the appropriate section of this
final rule to clarify that some of the 10 sites proposed for
development in the HSA overlap with those sites identified as
economically developable, and that none of the 10 proposed sites
includes streams with Pacific Hawaiian damselfly populations. We have
added the information regarding the proposed hydroelectric development
on the stream site associated with the only known location of the
flying earwig Hawaiian damselfly to our threats analysis (see Factor
A).
Summary of Factors Affecting the Species
Section 4 of the Act (16 U.S.C. 1531 et seq.) and its implementing
regulations (50 CFR part 424) set forth the procedures for adding
species to the Federal Lists of Endangered and Threatened Wildlife and
Plants. A species may be determined to be an endangered or threatened
species due to one or more of the five factors described in section
4(a)(1) of the Act. These five listing factors are: (A) The present or
threatened destruction, modification, or curtailment of its habitat or
range; (B) overutilization for commercial, recreational, scientific, or
educational purposes; (C) disease or predation; (D) the inadequacy of
existing regulatory mechanisms; and (E) other natural or manmade
factors affecting its continued existence. Listing actions may be
warranted based on any of the above threat factors, singly or in
combination.
The threats to the flying earwig and Pacific Hawaiian damselfly
species are summarized according to the five listing factors in Table
1, and discussed in detail below.
TABLE 1. SUMMARY OF THREATS TO THE FLYING EARWING HAWAIIAN DAMSELFLY AND PACIFIC HAWAIIAN DAMSELFLY.
----------------------------------------------------------------------------------------------------------------
SPECIES
-------------------------------------------------
5 FACTORS CATEGORY THREATS Flying Earwig Hawaiian Pacific Hawaiian
Damselfly Damselfly
----------------------------------------------------------------------------------------------------------------
FACTOR A Agriculture/urban X X
development
----------------------------------------------------------------------------------------------------------------
Stream alteration P X
----------------------------------------------------------------------------------------------------------------
Habitat modification by X --
pigs
----------------------------------------------------------------------------------------------------------------
Habitat modification by X X
nonnative plants
----------------------------------------------------------------------------------------------------------------
Stochastic events X X
----------------------------------------------------------------------------------------------------------------
Climate change P P
----------------------------------------------------------------------------------------------------------------
FACTOR B Overcollection P --
----------------------------------------------------------------------------------------------------------------
FACTOR C Predation A, BF (P) A, B, F, BF
----------------------------------------------------------------------------------------------------------------
FACTOR D Inadequate habitat X X
protection
----------------------------------------------------------------------------------------------------------------
Inadequate protection X X
from nonnative aquatic
species
----------------------------------------------------------------------------------------------------------------
FACTOR E Limited populations X X
----------------------------------------------------------------------------------------------------------------
A = ants
[[Page 35996]]
B = backswimmers
F = fish
BF = bullfrogs
P = potential threat
X = known threat
Factor A. The Present or Threatened Destruction, Modification, or
Curtailment of Its Habitat or Range
Freshwater habitats used by the flying earwig and Pacific Hawaiian
damselflies on all of the main Hawaiian Islands are severely altered
and degraded because of past and present land and water management
practices, including: agriculture and urban development; development of
groundwater, perched aquifer (aquifer sitting above main water table),
and surface water resources; and the deliberate and accidental
introductions of nonnative animals (Harris et al. 1993, pp. 12-13;
Meier et al. 1993, pp. 181-183).
Habitat Destruction and Modification by Agriculture and Urban
Development
Although there has not been a comprehensive, site-by-site
assessment of wetland loss in Hawaii (Erikson and Puttock 2006, p. 40),
Dahl (1990, p. 7) estimated that at least 12 percent of lowland to
upper-elevation wetlands in Hawaii had been converted to non-wetland
habitat by the 1980s. If only coastal plain (below 1,000 ft (305 m)
elevation) wetlands are considered, it is estimated that 30 percent
have been converted for agricultural and urban development (Kosaka
l990, p. 1). These marshlands and wetlands provided habitat for several
damselfly species, including the Pacific Hawaiian damselfly.
By the 1930s, water diversions had been developed on all of the
main Hawaiian Islands, and by 1978, the stream flow in over one-half of
all of the 366 perennial streams in Hawaii had been altered in some
manner (Brasher 2003, p. 1055). All or most of the low or average flow
of the stream was, and often still is, diverted into fields or
reservoirs, leaving many stream channels completely dry (Takasaki et
al. 1969, pp. 27-28; Harris et al. 1993, p. 12; Wilcox 1996, p. 56).
The historical destruction and modification of habitat continues to
impact the two Hawaiian damselflies, by restricting them to curtailed
or isolated habitat areas that are often degraded in quality (for
example, by the presence of predatory nonnative fishes). The present
curtailment of the habitat or range of the flying earwig Hawaiian
damselfly and Pacific Hawaiian damselfly due to past habitat
destruction or modification in turn limits population size,
distribution, and connectivity, resulting in an increased probability
of local extirpation or even extinction of the two Hawaiian damselfly
species.
Although extensive filling of freshwater wetlands is rarely
permitted today, loss of riparian or wetland habitats utilized by the
Pacific and flying earwig Hawaiian damselflies, such as smaller areas
of moist slopes, emergent vegetation, and narrow strips of freshwater
seeps within anchialine pool complexes (landlocked bodies of water with
a subterranean connection to the ocean), still occurs. In addition,
marshes have been, and continue to be, slowly filled and converted to
meadow habitat due to increased sedimentation resulting from increased
storm water runoff from upslope development, the accumulation of
uncontrolled growth of invasive vegetation, and blockage of downslope
drainage (Wilson Okamoto & Associates, Inc. 1993, pp. 3-4 to 3-5).
The effects of future conversion of wetland and other aquatic
habitat for agriculture and urban development are immediate and
significant for the following reason: As noted above, an estimated 30
percent of all coastal plain wetlands in Hawaii have already been lost
to agriculture and urban development, while the loss of lowland
freshwater habitat in Hawaii already approaches 80 to 90 percent
(Kosaka 1990, p. 1). Lacking the aquatic habitat features that the
damselflies require for essential life history needs, such as marshes,
ponds, and sidepools along streams (Pacific Hawaiian damselfly) and
riparian habitat (flying earwig Hawaiian damselfly), these modified
areas no longer support populations of these two Hawaiian damselflies.
Agriculture and urban development have thus contributed to the present
curtailment of the habitat of these two Hawaiian damselflies, and we
have no indication that this threat is likely to be significantly
ameliorated in the foreseeable future.
Habitat Destruction and Modification by Stream Diversion
Stream modifications began with the early Hawaiians, who diverted
water to irrigate taro. However, unlike modern stream diversions which
often completely dewater streams all year around, early diversions
often took no more than half the stream flow, and typically were
periodic to occasionally flood taro ponds at different times through
the year, rather than continuously flood them (Handy and Handy 1972,
pp. 58-59). The advent of plantation sugarcane cultivation led to far
more extensive stream diversions, with the first diversion built in
1856 on Kauai (Wilcox 1996, p. 54). These systems were designed to tap
water at upper elevations (above 984 ft (300 m)) by means of a concrete
weir in the stream (Wilcox 1996, p. 54). All or most of the low or
average flow of the stream was, and often still is, diverted into
fields or reservoirs, leaving many stream channels completely dry
(Takasaki et al. 1969, pp. 27-28; Harris et al. 1993, p. 12; Wilcox
1996, p. 56).
As noted above, by the 1930s, water diversions had been developed
on all of the main Hawaiian Islands, and by 1978, the stream flow in
over one-half of all of the 366 perennial streams in Hawaii had been
altered in some manner (Brasher 2003, p. 1055). Some stream diversion
systems are extensive, such as the Waiahole Ditch, which diverts water
from 37 streams within the range of the Pacific Hawaiian damselfly on
the windward side of Oahu to the dry plains on the leeward side of the
island via a tunnel cut through the Koolau mountain range (Stearns and
Vaksvik 1935, pp. 399-403). On west Maui, as of 1978, over 49 miles
(mi) (78 kilometers (km)) of stream habitat in 12 streams had been lost
due to diversions, and all of the 17 perennial streams on west Maui are
dewatered to some extent (Maciolek 1979, p. 605). This loss of stream
habitat may have contributed to the extirpation of the Pacific Hawaiian
damselfly population on west Maui. Given the affiliation of the flying
earwig Hawaiian damselfly with riparian habitats, this loss of stream
habitat may also potentially account for its absence on west Maui. Most
lower-elevation stream segments on west Maui are now completely dry,
except during storm-influenced flows (Maciolek 1979, p. 605).
The maintenance of natural hydrology is closely tied to the life
history requirements of the Hawaiian damselflies, as the presence of
standing or running water is essential to reproduction of the two
species. In addition to providing breeding habitat for the adults, the
aquatic larval stage of the Pacific Hawaiian damselfly is entirely
dependent on water, and the maintenance of local soil hydrology is
necessary for the persistence of uluhe
[[Page 35997]]
ferns, which provide habitat for the larval stage of the flying earwig
Hawaiian damselfly. The reduced flow or complete dewatering of streams
thus results in the destruction or degradation of habitat conditions
for both the Pacific and flying earwig Hawaiian damselflies. The
extensive diversion of streams on Maui island-wide has reduced the
amount of stream habitat available to the Pacific Hawaiian damselfly,
and potentially to the flying earwig Hawaiian damselfly as well.
In addition to diverting water for agriculture and domestic water
supply, streams in Hawaii have also been diverted for use in
hydroelectric power. In some cases, the water used for power generation
is already being diverted for another use; in other cases the water is
returned to the stream of origin. There are a total of 18 active
hydroelectric plants operating on Hawaiian streams on the islands of
Hawaii, Kauai, and Maui, only one of which is located on a stream where
a historical population of the Pacific Hawaiian damselfly was known on
Kauai (Waimea). Another 28 sites have been identified as feasible for
hydroelectric development on the islands of Hawaii, Kauai, Maui, and
Molokai (Hawaii Stream Assessment 1990, pp. xxi, 96-97). Three of the
sites identified as developable include current populations of the
Pacific Hawaiian damselfly. A total of 10 streams have actually been
proposed for development, with some overlap between the 28 streams
identified as feasible. Notably, the stream adjacent to the single
current remaining population site for the flying earwig Hawaiian
damselfly on Maui is included among those proposed for hydroelectric
development. Any additional diversion of stream flow for use in
hydroelectric power could contribute to further loss of stream habitat
for the Pacific Hawaiian damselfly and for the flying earwig Hawaiian
damselfly.
Habitat Modification and Destruction by Dewatering of Aquifers
In addition to the diversion of stream water and the resultant
downstream dewatering, many streams in Hawaii have experienced reduced
or zero surface flow as a result of the dewatering of their source
aquifers. Often these aquifers, which previously fed the streams, were
tapped by tunneling or the injudicious placement of wells (Stearns and
Vaksvik 1935, pp. 386-434; Stearns 1985, pp. 291-305). These
groundwater sources were captured for both domestic and agricultural
use and in some areas have completely depleted nearby stream and spring
flows. For example, the Waikolu Stream on Molokai has reduced flow due
in part to groundwater withdrawal (Brasher 2003, p. 1,056), which may
have reduced stream habitat available to the Pacific Hawaiian
damselfly. Likewise, on Maui, streams in the west Maui Mountains that
flow into the Lahaina District are fed by groundwater leaking from
breached high-elevation dikes. Downstream of the dike compartments,
stream diversions are designed to capture all of the low stream flow,
causing the streams downstream to be frequently dry (U.S. Geological
Survey 2008a, p. 1), likely impacting available habitat for the Pacific
Hawaiian damselfly, and potentially for the flying earwig Hawaiian
damselfly, in the Honolua and Honokohau streams.
The island of Lanai lies within the rain shadow of the west Maui
Mountains, which reach 5,788 ft (1,764 m) in elevation. Lower in
elevation than Maui, annual rainfall on Lanai's summit is 30 to 40 in
(760 to 1,015 mm), but is much less over the rest of the island
(University of Hawaii Department of Geography 1998, p. 13). Flows of
almost every spring and seep on Lanai have been diverted (Stearns 1940,
pp. 73-74, 85, 88, 95). Surface waters in streams have also been
diverted by tunnels in stream beds. Historically, Maunalei Stream was
the only perennial stream on Lanai, and Hawaiians constructed taro loi
(ponds for cultivation of taro) in the lower portions of this stream
system. In 1911, a tunnel was constructed at 1,100 ft (330 m) elevation
that undercuts the stream bed, diverting both the surface and
subsurface flows and dewatering the stream from this point to its mouth
(Stearns 1940, pp. 86-88). The Pacific Hawaiian damselfly, which
depends on stream habitat, was historically known from Lanai but is no
longer extant on this island. The Pacific Hawaiian damselfly was most
likely impacted by the dewatering of this stream because it was the
only permanent stream on Lanai prior to its dewatering. This example of
the negative impact of dewatering leads us to conclude that dewatering
poses a threat to the Pacific Hawaiian damselfly and the flying earwig
Hawaiian damselfly on the remaining islands where the species persist.
Habitat Modification and Destruction by Vertical Wells
Surface flow of streams has also been affected by vertical wells
drilled in the past, because the basal aquifer (lowest groundwater
layer) and alluvial caprock (sediment-deposited harder rock layer)
through which the lower sections of streams flow can be pierced and
hydraulically connected by wells (Stearns 1940, p. 88). This allows
water in aquifers normally feeding the stream to be diverted elsewhere
underground. Dewatering of the streams by tunneling and earlier, less-
informed well placement near or in streams was a significant cause of
habitat loss, and these effects continue today. Historically, for
example, there was sufficient surface flow in Makaha and Nanakuli
streams on Oahu to support taro loi in their lower reaches, but this
flow disappeared subsequent to construction of vertical wells upstream
(Devick 1995, p. 1). The inadvertent dewatering of streams through the
piercing of their aquifers (which are normally separated from adjacent
water-bearing layers by an impermeable layer), by tunneling or through
placement of vertical wells, caused the loss of Pacific Hawaiian
damselfly habitat, and contributed to the Pacific Hawaiian damselfly's
extirpation on the islands of Oahu, Kauai, and Lanai (Polhemus and
Asquith 1996, pp. 23-24). Such activities also reduced the extent of
stream habitat for the Pacific Hawaiian damselfly on the islands of
Maui, Molokai, and Hawaii. Most lower-elevation stream segments on west
Maui and leeward east Maui are now completely dry, except during storm-
influenced flows (Maciolek 1979, p. 605). The flow of nearly every seep
and spring on Lanai has been captured or bored with wells (Stearns
1940, pp. 73-74, 85, 88, 95). The inadvertent drying of streams from
earlier, uninformed well placement and other activities has contributed
to the decline of the Pacific Hawaiian damselfly by reducing its
habitat on all of the islands from which it was historically known. It
should be noted that the Pacific Hawaiian damselfly was once among the
most commonly observed aquatic insects in the islands (Howarth 1991, p.
40). The dewatering of streams on Maui and Hawaii may also have
impacted habitat of the flying earwig Hawaiian damselfly.
Although the State of Hawaii's Commission on Water Resource
Management is now more cognizant of the effects that groundwater
removal has on streams via injudicious placement of wells, the
Commission still routinely reviews new permit applications for wells
(Hardy 2009, p. 1). Thus, the potential for additional well-drilling
continues to be a threat (see further discussion under Factor D, The
Inadequacy of Existing Regulatory Mechanisms, below), and the ongoing
effects of previously constructed vertical wells continue to be an
ongoing threat to the Hawaiian dragonflies.
[[Page 35998]]
Habitat Modification and Destruction by Channelization
In addition to the destruction of most of the stream habitat of the
Pacific Hawaiian damselfly and the flying earwig Hawaiian damselfly,
much of the remaining stream habitat has been, and continues to be,
seriously degraded throughout the Hawaiian Islands. Stream degradation
has been particularly severe on the island of Oahu where, by 1978, 58
percent of all the perennial streams had been channelized (lined,
partially lined, or altered) to control flooding (Brasher 2003, p.
1055; Polhemus and Asquith 1996, p. 24), and 89 percent of the total
length of these streams had been channelized (Parrish et al. 1984, p.
83). The channelization of streams creates artificial, wide-bottomed
stream beds and often results in removal of riparian vegetation,
increased substrate homogeneity, increased temporal water velocity
(increased water flow speed during times of higher precipitation,
including minor and major flooding), increased illumination, and higher
water temperatures (Parrish et al. 1984, p. 83; Brasher 2003, p. 1052).
Natural streams meander and are lined with rocks, trees, and natural
debris, and during times of flooding, jump their banks. Channelized
streams are straightened and often lack natural obstructions, and
during times of higher precipitation or flooding, facilitate a higher
water flow velocity. Hawaiian damselflies are largely absent from
channelized portions of streams (Polhemus and Asquith 1996, p. 24). In
contrast, undisturbed Hawaiian stream systems exhibit a greater amount
of riffle habitat, canopy closure, higher consistent flow velocity, and
lower water temperatures that are characteristic of streams to which
the Hawaiian damselflies, in general, are adapted (Brasher 2003, pp.
1054-1057).
Channelization of streams has not been restricted to lower stream
reaches. For example, there is extensive channelization of the Kalihi
Stream, on the island of Oahu, above 1,000-ft (300-m) elevation.
Extensive stream channelization has contributed to the extirpation of
the Pacific Hawaiian damselfly on Oahu (Englund 1999, p. 236; Polhemus
2008, pp. 45-46).
Stream diversion, channelization, and dewatering represent
significant and immediate threats to the Pacific Hawaiian damselfly for
the following reasons: (1) They reduce the amount and distribution of
stream habitat available to this species; (2) they reduce stream flow,
leaving lower elevation stream segments completely dry except during
storms, or leaving many streams completely dry year-round, thus
reducing or eliminating stream habitat; and (3) they indirectly lead to
an increase in water temperature that leads to the loss of Pacific
Hawaiian damselfly naiads due to direct physiological stress. Because
the probability of species extinction increases when ranges are
restricted, habitat decreases, and population numbers decline, the
Pacific Hawaiian damselfly is particularly vulnerable to extinction due
to such changes in its stream habitats.
In addition, stream diversion, dewatering, and vertical wells have
the potential to negatively impact, and in some cases may have
impacted, the flying earwig Hawaiian damselfly. Stream flow is
essential to the adult flying earwig damselfly's breeding requirements
and is also essential to maintaining localized soil hydrology necessary
for persistence of uluhe ferns, which are known foraging and mating
sites for the adults and may provide habitat for the larval stage.
Should the species' population site stream experience either reduced
flow or complete dewatering for an extended period of time, it is
expected that the impact to surrounding soils and associated
vegetation, including the uluhe ferns that are believed to be the
species' likely larval-stage habitat, will be soil desiccation and
prolonged vegetation dieback, respectively.
Habitat Destruction and Modification by Feral Pigs
One of the primary threats to the flying earwig Hawaiian damselfly
is the ongoing destruction and degradation of its riparian habitat by
nonnative animals, particularly feral pigs (Sus scrofa) (Polhemus and
Asquith 1996, p. 22; Erickson and Puttock 2006, p. 42). Pigs of Asian
descent were first introduced to Hawaii by the Polynesian ancestors of
Hawaiians around 400 A.D. (Kirch 1982, pp. 3-4). Western immigrants,
beginning with Captain Cook in 1778, repeatedly introduced European
strains (Tomich 1986, pp. 120-121). The pigs escaped domestication and
successfully invaded all areas, including wet and mesic forests and
grasslands, on all of the main Hawaiian Islands.
High pig densities and expansion of their distribution have caused
indisputable widespread damage to native vegetation on the Hawaiian
Islands (Cuddihy and Stone 1990, p. 63). Feral pigs create open areas
within forest habitat by digging up, eating, and trampling native plant
species (Stone 1985, p. 263). These open areas become fertile ground
for nonnative plant seeds spread through the excrement of the pigs and
by transport in their hair (Stone 1985, p. 263). In nitrogen-poor
soils, feral pig excrement increases nutrient availability, enhancing
establishment of nonnative weeds that are more adapted to richer soils
than are native plants (Cuddihy and Stone 1990, p. 65). In this manner,
largely nonnative forests replace native forest habitat (Cuddihy and
Stone 1990, p. 65). In addition, feral pigs will root and dig for plant
tubers and worms in wetlands, including marshes, on all of the main
Hawaiian Islands (Erikson and Puttock 2006, p. 42).
In a study conducted in the 1980s on feral pig populations in
Kipahulu Valley on Maui, the deleterious effects of feral pig rooting
on native forest ecosystems was documented (Diong 1982, pp. 150, 160-
167). Rooting by feral pigs was observed to be related to the search
for earthworms, with rooting depths averaging 8 in (20 cm), and rooting
was found to greatly disrupt the leaf litter and topsoil layers, and
contribute to erosion and changes in ground topography. The feeding
habits of pigs were observed to create seed beds, enabling the
establishment and spread of invasive weedy species such as Clidemia
hirta (Koster's curse). The study concluded that all aspects of the
feeding habits of pigs are damaging to the structure and function of
the Hawaiian forest ecosystem (Diong 1982, pp. 160-167).
It is likely that pigs similarly impact the native vegetation used
for perching by adult flying earwig Hawaiian damselflies. On Maui,
feral pigs inhabit the uluhe-dominated riparian habitat of the flying
earwig Hawaiian damselfly. Thro